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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
10-Q
☒ |
QUARTERLY
REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For
the quarterly period ended September 30, 2023
or
☐ |
TRANSITION
REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For
the transition period from ________ to ________
Commission
File Number 001-39678
SANARA
MEDTECH INC.
(Exact
name of Registrant as specified in its charter)
Texas |
|
59-2219994 |
(State
or other jurisdiction of |
|
(I.R.S.
Employer |
incorporation
or organization) |
|
Identification
No.) |
1200
Summit Ave, Suite 414, Fort Worth, Texas 76102
(Address
of principal executive offices)
(817)
529-2300
(Registrant’s
telephone number, including area code)
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on which registered |
Common
Stock, $0.001 par value |
|
SMTI |
|
The
Nasdaq Capital Market |
Indicate
by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange
Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)
has been subject to such filing requirements for the past 90 days. ☒Yes☐ No
Indicate
by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule
405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant
was required to submit such files). ☒Yes ☐ No
Indicate
by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting
company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,”
“smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large
accelerated filer |
Accelerated
filer |
Non-accelerated
filer |
Smaller
reporting company |
Emerging
growth company |
☐ |
☐ |
☒ |
☒ |
☐ |
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate
by check mark whether registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
As
of November 13, 2023, 8,538,489
shares of the Issuer’s common stock, $0.001 par value
per share, were outstanding.
SANARA
MEDTECH INC.
Form
10-Q
Quarter
Ended September 30, 2023
Sanara,
Sanara MedTech, our logo and our other trademarks or service marks appearing in this report are the property of Sanara MedTech Inc. Trade
names, trademarks and service marks of other companies appearing in this report are the property of their respective owners. Solely for
convenience, the trademarks, service marks and trade names included in this report are without the ®, ™ or other applicable
symbols, but such references are not intended to indicate, in any way, that we will not assert, to the fullest extent under applicable
law, our rights or the rights of the applicable licensors to these trademarks, service marks and trade names.
Unless
otherwise indicated, “Sanara MedTech,” “Sanara,” “the Company,” “our,” “us,”
or “we,” refer to Sanara MedTech Inc. and its consolidated subsidiaries.
Part
I – Financial Information
ITEM
1. FINANCIAL STATEMENTS
SANARA
MEDTECH INC. AND SUBSIDIARIES
CONSOLIDATED
BALANCE SHEETS
| |
(Unaudited) | | |
| |
| |
September 30, 2023 | | |
December 31, 2022 | |
Assets | |
| | |
| |
Current assets | |
| | | |
| | |
Cash | |
$ | 6,235,912 | | |
$ | 8,958,995 | |
Accounts receivable, net | |
| 7,436,295 | | |
| 6,805,761 | |
Accounts receivable – related party | |
| 11,032 | | |
| 98,548 | |
Accounts receivable | |
| 11,032 | | |
| 98,548 | |
Royalty receivable | |
| 49,344 | | |
| 99,594 | |
Inventory, net | |
| 5,021,030 | | |
| 3,549,000 | |
Prepaid and other assets | |
| 621,690 | | |
| 1,104,611 | |
Total current assets | |
| 19,375,303 | | |
| 20,616,509 | |
| |
| | | |
| | |
Long-term assets | |
| | | |
| | |
Property and equipment, net | |
| 1,327,056 | | |
| 1,416,436 | |
Right of use assets – operating leases | |
| 2,094,188 | | |
| 806,402 | |
Goodwill | |
| 3,601,781 | | |
| 3,601,781 | |
Intangible assets, net | |
| 45,991,466 | | |
| 31,509,980 | |
Investment in equity securities | |
| 3,084,278 | | |
| 3,084,278 | |
Total long-term assets | |
| 56,098,769 | | |
| 40,418,877 | |
| |
| | | |
| | |
Total assets | |
$ | 75,474,072 | | |
$ | 61,035,386 | |
| |
| | | |
| | |
Liabilities and shareholders’ equity | |
| | | |
| | |
Current liabilities | |
| | | |
| | |
Accounts payable | |
$ | 1,939,887 | | |
$ | 1,392,701 | |
Accounts payable – related parties | |
| 64,747 | | |
| 34,036 | |
Accounts payable | |
| 64,747 | | |
| 34,036 | |
Accrued royalties and expenses | |
| 3,583,439 | | |
| 2,144,475 | |
Accrued bonuses and commissions | |
| 6,084,654 | | |
| 7,758,284 | |
Earnout liabilities – current | |
| 1,000,000 | | |
| 1,162,880 | |
Operating lease liabilities – current | |
| 322,206 | | |
| 313,933 | |
Current portion of debt | |
| 232,143 | | |
| - | |
Total current liabilities | |
| 13,227,076 | | |
| 12,806,309 | |
| |
| | | |
| | |
Long-term liabilities | |
| | | |
| | |
Earnout liabilities – long-term | |
| 4,871,986 | | |
| 6,003,811 | |
Operating lease liabilities – long-term | |
| 1,846,293 | | |
| 505,291 | |
Long-term debt, net of current portion | |
| 9,458,254 | | |
| - | |
Other long-term liabilities | |
| 1,972,673 | | |
| - | |
Total long-term liabilities | |
| 18,149,206 | | |
| 6,509,102 | |
| |
| | | |
| | |
Total liabilities | |
| 31,376,282 | | |
| 19,315,411 | |
| |
| | | |
| | |
Commitments and contingencies (Note 10) | |
| - | | |
| - | |
| |
| | | |
| | |
Shareholders’ equity | |
| | | |
| | |
Common Stock: $0.001 par value, 20,000,000 shares authorized; 8,540,226 issued and outstanding as of September 30, 2023 and 8,299,957 issued and outstanding as of December 31, 2022 | |
| 8,540 | | |
| 8,300 | |
Additional paid-in capital | |
| 72,107,881 | | |
| 65,213,987 | |
Accumulated deficit | |
| (27,799,621 | ) | |
| (23,394,757 | ) |
Total Sanara MedTech shareholders’ equity | |
| 44,316,800 | | |
| 41,827,530 | |
Equity attributable to noncontrolling interest | |
| (219,010 | ) | |
| (107,555 | ) |
Total shareholders’ equity | |
| 44,097,790 | | |
| 41,719,975 | |
Total liabilities and shareholders’ equity | |
$ | 75,474,072 | | |
$ | 61,035,386 | |
The
accompanying notes are an integral part of these unaudited consolidated financial statements.
SANARA
MEDTECH INC. AND SUBSIDIARIES
CONSOLIDATED
STATEMENTS OF OPERATIONS (UNAUDITED)
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
| | |
| | |
| | |
| |
Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
| |
| | | |
| | | |
| | | |
| | |
Cost of goods sold | |
| 1,751,349 | | |
| 2,228,561 | | |
| 6,064,524 | | |
| 3,991,728 | |
| |
| | | |
| | | |
| | | |
| | |
Gross profit | |
| 14,273,599 | | |
| 10,816,010 | | |
| 41,235,505 | | |
| 26,534,844 | |
| |
| | | |
| | | |
| | | |
| | |
Operating expenses | |
| | | |
| | | |
| | | |
| | |
Selling, general and administrative expenses | |
| 13,877,879 | | |
| 12,062,195 | | |
| 40,658,424 | | |
| 31,865,958 | |
Research and development | |
| 986,454 | | |
| 1,061,387 | | |
| 3,480,906 | | |
| 2,333,024 | |
Depreciation and amortization | |
| 997,674 | | |
| 814,881 | | |
| 2,580,243 | | |
| 1,556,752 | |
Change in fair value of earnout liabilities | |
| (681,753 | ) | |
| 109,689 | | |
| (1,494,910 | ) | |
| 173,116 | |
Total operating expenses | |
| 15,180,254 | | |
| 14,048,152 | | |
| 45,224,663 | | |
| 35,928,850 | |
| |
| | | |
| | | |
| | | |
| | |
Operating loss | |
| (906,655 | ) | |
| (3,232,142 | ) | |
| (3,989,158 | ) | |
| (9,394,006 | ) |
| |
| | | |
| | | |
| | | |
| | |
Other expense | |
| | | |
| | | |
| | | |
| | |
Interest expense and other | |
| (188,294 | ) | |
| - | | |
| (188,300 | ) | |
| - | |
Share of losses from equity method investment | |
| - | | |
| - | | |
| - | | |
| (379,633 | ) |
Total other expense | |
| (188,294 | ) | |
| - | | |
| (188,300 | ) | |
| (379,633 | ) |
| |
| | | |
| | | |
| | | |
| | |
Income tax benefit | |
| - | | |
| 1,702,890 | | |
| - | | |
| 5,844,796 | |
| |
| | | |
| | | |
| | | |
| | |
Net loss | |
| (1,094,949 | ) | |
| (1,529,252 | ) | |
| (4,177,458 | ) | |
| (3,928,843 | ) |
| |
| | | |
| | | |
| | | |
| | |
Less: Net loss attributable to noncontrolling interest | |
| (34,579 | ) | |
| (58,792 | ) | |
| (111,455 | ) | |
| (98,485 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss attributable to Sanara MedTech shareholders | |
$ | (1,060,370 | ) | |
$ | (1,470,460 | ) | |
$ | (4,066,003 | ) | |
$ | (3,830,358 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss per share of common stock, basic and diluted | |
$ | (0.13 | ) | |
$ | (0.18 | ) | |
$ | (0.49 | ) | |
$ | (0.49 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of common shares outstanding, basic and diluted | |
| 8,332,341 | | |
| 8,107,261 | | |
| 8,244,503 | | |
| 7,836,882 | |
The
accompanying notes are an integral part of these unaudited consolidated financial statements.
SANARA
MEDTECH INC. AND SUBSIDIARIES
CONSOLIDATED
STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY (UNAUDITED)
| |
Shares | | |
Amount | | |
Capital | | |
Deficit | | |
Interest | | |
Equity | |
| |
Common Stock | | |
Additional | | |
| | |
| | |
Total | |
| |
$0.001 par value | | |
Paid-In | | |
Accumulated | | |
Noncontrolling | | |
Shareholders’ | |
| |
Shares | | |
Amount | | |
Capital | | |
Deficit | | |
Interest | | |
Equity | |
Balance at December 31, 2021 | |
| 7,676,662 | | |
$ | 7,677 | | |
$ | 45,867,768 | | |
$ | (15,235,044 | ) | |
$ | (488,397 | ) | |
$ | 30,152,004 | |
Share-based compensation | |
| 137,076 | | |
| 136 | | |
| 1,622,982 | | |
| - | | |
| - | | |
| 1,623,118 | |
Net settlement and retirement of equity-based awards | |
| (3,343 | ) | |
| (3 | ) | |
| (52,284 | ) | |
| (50,644 | ) | |
| - | | |
| (102,931 | ) |
Net loss | |
| - | | |
| - | | |
| - | | |
| (3,129,324 | ) | |
| (27,181 | ) | |
| (3,156,505 | ) |
Balance at March 31, 2022 | |
| 7,810,395 | | |
| 7,810 | | |
| 47,438,466 | | |
| (18,415,012 | ) | |
| (515,578 | ) | |
| 28,515,686 | |
Share-based compensation | |
| 39,268 | | |
| 39 | | |
| 703,361 | | |
| - | | |
| - | | |
| 703,400 | |
Issuance of common stock for acquisitions | |
| 165,738 | | |
| 166 | | |
| 5,096,278 | | |
| - | | |
| - | | |
| 5,096,444 | |
Issuance of common stock options and warrants for acquisitions | |
| - | | |
| - | | |
| 4,612,645 | | |
| - | | |
| - | | |
| 4,612,645 | |
Distribution to noncontrolling interest member | |
| - | | |
| - | | |
| - | | |
| - | | |
| (220,000 | ) | |
| (220,000 | ) |
Net income (loss) | |
| - | | |
| - | | |
| - | | |
| 769,426 | | |
| (12,512 | ) | |
| 756,914 | |
Balance at June 30, 2022 | |
| 8,015,401 | | |
| 8,015 | | |
| 57,850,750 | | |
| (17,645,586 | ) | |
| (748,090 | ) | |
| 39,465,089 | |
Share-based compensation | |
| (3,358 | ) | |
| (3 | ) | |
| 683,205 | | |
| - | | |
| - | | |
| 683,202 | |
Issuance of common stock for acquisitions | |
| 291,686 | | |
| 292 | | |
| 6,031,775 | | |
| - | | |
| (2,638 | ) | |
| 6,029,429 | |
Net loss | |
| - | | |
| - | | |
| - | | |
| (1,470,460 | ) | |
| (58,792 | ) | |
| (1,529,252 | ) |
Balance at September 30, 2022 | |
| 8,303,729 | | |
$ | 8,304 | | |
$ | 64,565,730 | | |
$ | (19,116,046 | ) | |
$ | (809,520 | ) | |
$ | 44,648,468 | |
| |
Common Stock | | |
Additional | | |
| | |
| | |
Total | |
| |
$0.001 par value | | |
Paid-In | | |
Accumulated | | |
Noncontrolling | | |
Shareholders’ | |
| |
Shares | | |
Amount | | |
Capital | | |
Deficit | | |
Interest | | |
Equity | |
Balance at December 31, 2022 | |
| 8,299,957 | | |
$ | 8,300 | | |
$ | 65,213,987 | | |
$ | (23,394,757 | ) | |
$ | (107,555 | ) | |
$ | 41,719,975 | |
Share-based compensation | |
| 74,781 | | |
| 75 | | |
| 597,230 | | |
| - | | |
| - | | |
| 597,305 | |
Net settlement and retirement of equity-based awards | |
| (15,854 | ) | |
| (16 | ) | |
| (315,572 | ) | |
| (340,354 | ) | |
| - | | |
| (655,942 | ) |
Issuance of common stock in equity offering | |
| 26,143 | | |
| 26 | | |
| 1,033,735 | | |
| - | | |
| - | | |
| 1,033,761 | |
Net loss | |
| - | | |
| - | | |
| - | | |
| (1,177,900 | ) | |
| (38,429 | ) | |
| (1,216,329 | ) |
Balance at March 31, 2023 | |
| 8,385,027 | | |
| 8,385 | | |
| 66,529,380 | | |
| (24,913,011 | ) | |
| (145,984 | ) | |
| 41,478,770 | |
Share-based compensation | |
| 33,355 | | |
| 33 | | |
| 1,127,299 | | |
| - | | |
| - | | |
| 1,127,332 | |
Net settlement and retirement of equity-based awards | |
| 21,363 | | |
| 22 | | |
| 224,740 | | |
| (186 | ) | |
| - | | |
| 224,576 | |
Net loss | |
| - | | |
| - | | |
| - | | |
| (1,827,733 | ) | |
| (38,447 | ) | |
| (1,866,180 | ) |
Balance at June 30, 2023 | |
| 8,439,745 | | |
| 8,440 | | |
| 67,881,419 | | |
| (26,740,930 | ) | |
| (184,431 | ) | |
| 40,964,498 | |
Balance | |
| 8,439,745 | | |
$ | 8,440 | | |
$ | 67,881,419 | | |
$ | (26,740,930 | ) | |
$ | (184,431 | ) | |
$ | 40,964,498 | |
Share-based compensation | |
| (339 | ) | |
| (1 | ) | |
| 857,527 | | |
| - | | |
| - | | |
| 857,526 | |
Net settlement and retirement of equity-based awards | |
| 27,011 | | |
| 27 | | |
| 279,364 | | |
| 1,679 | | |
| - | | |
| 281,070 | |
Issuance of common stock for acquisitions | |
| 73,809 | | |
| 74 | | |
| 3,089,571 | | |
| - | | |
| - | | |
| 3,089,645 | |
Net loss | |
| - | | |
| - | | |
| - | | |
| (1,060,370 | ) | |
| (34,579 | ) | |
| (1,094,949 | ) |
Net income (loss) | |
| - | | |
| - | | |
| - | | |
| (1,060,370 | ) | |
| (34,579 | ) | |
| (1,094,949 | ) |
Balance at September 30, 2023 | |
| 8,540,226 | | |
$ | 8,540 | | |
$ | 72,107,881 | | |
$ | (27,799,621 | ) | |
$ | (219,010 | ) | |
$ | 44,097,790 | |
Balance | |
| 8,540,226 | | |
$ | 8,540 | | |
$ | 72,107,881 | | |
$ | (27,799,621 | ) | |
$ | (219,010 | ) | |
$ | 44,097,790 | |
The
accompanying notes are an integral part of these unaudited consolidated financial statements.
SANARA
MEDTECH INC. AND SUBSIDIARIES
CONSOLIDATED
STATEMENTS OF CASH FLOWS (UNAUDITED)
| |
2023 | | |
2022 | |
| |
Nine Months Ended | |
| |
September 30, | |
| |
2023 | | |
2022 | |
| |
| | |
| |
Cash flows from operating activities: | |
| | | |
| | |
Net loss | |
$ | (4,177,458 | ) | |
$ | (3,928,843 | ) |
Adjustments to reconcile net loss to net cash used in operating activities: | |
| | | |
| | |
Depreciation and amortization | |
| 2,580,243 | | |
| 1,556,752 | |
Loss on disposal of property and equipment | |
| - | | |
| 2,876 | |
Bad debt expense | |
| 214,061 | | |
| 220,000 | |
Inventory obsolescence | |
| 222,691 | | |
| 289,406 | |
Share-based compensation | |
| 2,582,163 | | |
| 1,971,537 | |
Noncash lease expense | |
| 243,988 | | |
| 189,409 | |
Loss on equity method investment | |
| - | | |
| 379,633 | |
Benefit from deferred income taxes | |
| - | | |
| (5,844,796 | ) |
Accretion of finance liabilities | |
| 39,699 | | |
| - | |
Amortization of debt issuance costs | |
| 2,055 | | |
| - | |
Change in fair value of earnout liabilities | |
| (1,494,910 | ) | |
| 173,116 | |
Changes in operating assets and liabilities: | |
| | | |
| | |
Accounts receivable, net | |
| (794,344 | ) | |
| (754,934 | ) |
Accounts receivable – related party | |
| 87,516 | | |
| 10,920 | |
Inventory, net | |
| (1,664,714 | ) | |
| (451,838 | ) |
Prepaid and other assets | |
| 482,921 | | |
| (69,490 | ) |
Accounts payable | |
| 547,186 | | |
| (800,788 | ) |
Accounts payable – related parties | |
| 30,711 | | |
| (126,812 | ) |
Accrued royalties and expenses | |
| 557,295 | | |
| 947,130 | |
Accrued bonuses and commissions | |
| (1,673,629 | ) | |
| 1,516,858 | |
Operating lease liabilities | |
| (182,498 | ) | |
| (189,990 | ) |
Net cash used in operating activities | |
| (2,397,024 | ) | |
| (4,909,854 | ) |
Cash flows from investing activities: | |
| | | |
| | |
Purchases of property and equipment | |
| (210,970 | ) | |
| (93,651 | ) |
Proceeds from disposal of property and equipment | |
| 650 | | |
| 894 | |
Purchases of intangible assets | |
| - | | |
| (600,000 | ) |
Investment in equity securities | |
| - | | |
| (250,000 | ) |
Acquisitions, net of cash acquired | |
| (9,942,750 | ) | |
| (2,191,919 | ) |
Net cash used in investing activities | |
| (10,153,070 | ) | |
| (3,134,676 | ) |
Cash flows from financing activities: | |
| | | |
| | |
Loan proceeds, net | |
| 9,688,341 | | |
| - | |
Equity offering net proceeds | |
| 1,033,761 | | |
| - | |
Net settlement of equity-based awards | |
| (150,296 | ) | |
| (102,931 | ) |
Cash payment of finance and earnout liabilities | |
| (744,795 | ) | |
| - | |
Distribution to noncontrolling interest member | |
| - | | |
| (220,000 | ) |
Net cash provided by (used in) financing activities | |
| 9,827,011 | | |
| (322,931 | ) |
Net decrease in cash | |
| (2,723,083 | ) | |
| (8,367,461 | ) |
Cash, beginning of period | |
| 8,958,995 | | |
| 18,652,841 | |
Cash, end of period | |
$ | 6,235,912 | | |
$ | 10,285,380 | |
| |
| | | |
| | |
Cash paid during the period for: | |
| | | |
| | |
Interest | |
$ | 146,546 | | |
$ | - | |
Supplemental noncash investing and financing activities: | |
| | | |
| | |
Right of use assets obtained in exchange for lease obligations | |
| 1,531,773 | | |
| - | |
Equity issued for acquisitions | |
| 3,089,645 | | |
| 15,738,518 | |
Earnout and other liabilities generated by acquisitions | |
| 3,759,642 | | |
| 6,882,151 | |
Investment in equity securities converted in asset acquisition | |
| - | | |
| 1,803,440 | |
The
accompanying notes are an integral part of these unaudited consolidated financial statements.
SANARA
MEDTECH INC. AND SUBSIDIARIES
NOTES
TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS
NOTE
1 – NATURE OF BUSINESS AND BACKGROUND
Sanara
MedTech Inc. (together with its wholly owned and majority-owned subsidiaries on a consolidated basis, the “Company”) is a
medical technology company focused on developing and commercializing transformative technologies to improve clinical outcomes and reduce
healthcare expenditures in the surgical, chronic wound and skincare markets. Each of the Company’s products, services and technologies
contributes to the Company’s overall goal of achieving better clinical outcomes at a lower overall cost for patients regardless
of where they receive care. The Company strives to be one of the most innovative and comprehensive providers of effective surgical, wound
and skincare solutions and is continually seeking to expand its offerings for patients requiring treatments across the entire continuum
of care in the United States.
NOTE
2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Principles
of Consolidation and Basis of Presentation
The
accompanying unaudited consolidated financial statements include the accounts of Sanara MedTech Inc. and its wholly owned and majority-owned
subsidiaries, as well as other entities in which the Company has a controlling financial interest. All significant intercompany profits,
losses, transactions and balances have been eliminated in consolidation. Certain prior year amounts have been reclassified to conform
to the current year presentation.
The
accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles
for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include
all the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. In the
opinion of management of the Company, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation
have been included. Operating results for interim periods are not necessarily indicative of the results that may be expected for the
full year period. These financial statements and notes should be read in conjunction with the financial statements for each of the two
years ended December 31, 2022 and 2021, which are included in the Company’s most recent Annual Report on Form 10-K.
Use
of Estimates
The
preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates
and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date
of the consolidated financial statements, and the reported revenue and expenses during the reporting period. However, actual results
could differ from those estimates and there may be changes to the Company’s estimates in future periods.
Cash
and Cash Equivalents
The
Company considers all highly liquid investments purchased with an original maturity of three months or less to be cash equivalents.
Income/Loss
Per Share
The
Company computes income/loss per share in accordance with Accounting Standards Codification (“ASC”) Topic 260, Earnings per
Share, which requires the Company to present basic and diluted income per share when the effect is dilutive. Basic income per share is
computed by dividing income available to common shareholders by the weighted average number of shares of common stock outstanding. Diluted
income per share is computed similarly to basic income per share, except that the denominator is increased to include the number of additional
shares of common stock that would have been outstanding if the potential shares of common stock had been issued and if the additional
shares of common stock were dilutive. All common stock equivalents were excluded from the calculations for the periods presented as their
inclusion would have been anti-dilutive during the three and nine months ended September 30, 2023 and 2022 due to the Company’s
net loss.
The
following table summarizes the shares of common stock that were potentially issuable but were excluded from the computation of diluted
net loss per share for the nine months ended September 30, 2023 and 2022, as such shares would have had an anti-dilutive effect:
SCHEDULE
OF COMPUTATION OF DILUTED NET LOSS PER SHARE
| |
2023 | | |
2022 | |
| |
As of September 30, | |
| |
2023 | | |
2022 | |
Stock options (a) | |
| 95,873 | | |
| 155,691 | |
Warrants (b) | |
| 16,725 | | |
| 16,725 | |
Unvested restricted stock | |
| 159,557 | | |
| 192,215 | |
Anti-dilutive securities | |
| 159,557 | | |
| 192,215 | |
Revenue
Recognition
The
Company recognizes revenue in accordance with ASC Topic 606, Revenue from Contracts with Customers (“ASC 606”). Revenues
are recognized when a purchase order is received from the customer and control of the promised goods or services is transferred to the
customer in an amount that reflects the consideration the Company expects to be entitled to receive in exchange for transferring those
goods or services. Revenue is recognized based on the following five-step model:
-
Identification of the contract with a customer
-
Identification of the performance obligations in the contract
-
Determination of the transaction price
-
Allocation of the transaction price to the performance obligations in the contract
-
Recognition of revenue when, or as, the Company satisfies a performance obligation
Details
of this five-step process are as follows:
Identification
of the contract with a customer
Customer
purchase orders are generally considered to be contracts under ASC 606. Purchase orders typically identify the specific terms of products
to be delivered, create the enforceable rights and obligations of both parties and result in commercial substance. No other forms of
contract revenue recognition, such as the completed contract or percentage of completion methods, were utilized by the Company in either
2023 or 2022.
Performance
obligations
The
Company’s performance obligation is generally limited to delivery of the requested items to its customers at the agreed upon quantities
and prices.
Determination
and allocation of the transaction price
The
Company has established prices for its products. These prices are effectively agreed to when customers place purchase orders with the
Company. Rebates and discounts, if any, are recognized in full at the time of sale as a reduction of net revenue. Allocation of transaction
prices is not necessary where only one performance obligation exists.
Recognition
of revenue as performance obligations are satisfied
Product
revenues are recognized when a purchase order is received from the customer, the products are delivered and control of the goods and
services passes to the customer.
Disaggregation
of Revenue
Revenue
streams from product sales and royalties are summarized below for the three and nine months ended September 30, 2023 and 2022.
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Soft tissue repair products | |
$ | 13,634,316 | | |
$ | 10,969,271 | | |
$ | 39,756,539 | | |
$ | 28,296,919 | |
Bone fusion products | |
| 2,340,382 | | |
| 2,025,050 | | |
| 7,392,740 | | |
| 2,078,903 | |
Royalty revenue | |
| 50,250 | | |
| 50,250 | | |
| 150,750 | | |
| 150,750 | |
Total Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
The
Company recognizes royalty revenue from a development and license agreement with BioStructures, LLC. The Company records revenue each
calendar quarter as earned per the terms of the agreement, which stipulates the Company will receive quarterly royalty payments of at
least $50,250. Under the terms of the development and license agreement, royalties of 2.0% are recognized on sales of products containing
the Company’s patented resorbable bone hemostasis. The minimum annual royalty due to the Company is $201,000 per year through the
end of 2023. These royalties are payable in quarterly installments of $50,250. To date, royalties related to this development and license
agreement have not exceeded the annual minimum of $201,000 ($50,250 per quarter).
Accounts
Receivable Allowances
Accounts
receivable are typically due within 30 days of invoicing. The Company establishes an allowance for doubtful accounts to provide for an
estimate of accounts receivable which are not expected to be collectible. The Company bases the allowance on an assessment of customer
creditworthiness, historical payment experience, the age of outstanding receivables and other information as applicable. The Company
recorded bad debt expense of $128,061 and $25,000 during the three months ended September 30, 2023 and 2022, respectively, and $214,061
and $220,000 during the nine months ended September 30, 2023 and 2022, respectively. The allowance for doubtful accounts was $511,089
at September 30, 2023 and $265,089 at December 31, 2022. The Company also establishes other allowances to provide for estimated customer
rebates and other expected customer deductions. These allowances totaled $5,297 at September 30, 2023 and $4,761 at December 31, 2022.
If circumstances related to customers change, estimates of the recoverability of receivables would be further adjusted.
Inventories
Inventories are stated at the lower
of cost or net realizable value, with cost computed on a first-in, first-out basis. Inventories consist primarily of finished goods,
and also include an immaterial amount of raw materials and related packaging components. The Company recorded inventory obsolescence
expense of $152,701
and $129,689
for the three months ended September 30, 2023 and 2022, respectively, and $222,691
and $289,406
for the nine months ended September 30, 2023 and 2022, respectively. The allowance for obsolete and slow-moving inventory had a
balance of $327,492
at September 30, 2023, and $523,832 at
December 31, 2022.
Property
and Equipment
Property
and equipment are stated at cost, less accumulated depreciation. Depreciation is recorded using the straight-line method over the estimated
useful lives of the related assets, ranging from two to ten years. Below is a summary of property and equipment for the periods presented:
SCHEDULE OF PROPERTY AND EQUIPMENT
| |
Useful | | |
September 30, | | |
December 31, | |
| |
Life | | |
2023 | | |
2022 | |
Computers | |
| 3-5 years | | |
$ | 194,788 | | |
$ | 172,154 | |
Office equipment | |
| 3-7 years | | |
| 154,280 | | |
| 87,225 | |
Furniture and fixtures | |
| 5-10 years | | |
| 323,755 | | |
| 258,414 | |
Leasehold improvements | |
| 2-5 years | | |
| 107,983 | | |
| 19,631 | |
Internal use software | |
| 5 years | | |
| 1,618,998 | | |
| 1,618,998 | |
Property and equipment, gross | |
| | | |
| 2,399,804 | | |
| 2,156,422 | |
Less accumulated depreciation | |
| | | |
| (1,072,748 | ) | |
| (739,986 | ) |
Property and equipment, net | |
| | | |
$ | 1,327,056 | | |
$ | 1,416,436 | |
Depreciation
expense related to property and equipment was $116,596 and $106,347 for the three months ended September 30, 2023 and 2022, respectively,
and $332,762 and $300,655 for the nine months ended September 30, 2023 and 2022, respectively.
Internal
Use Software
The
Company accounts for costs incurred to develop or acquire computer software for internal use in accordance with ASC Topic 350-40, Intangibles
– Goodwill and Other. The Company capitalizes the costs incurred during the application development stage, which generally includes
third-party developer fees to design the software configuration and interfaces, coding, installation and testing.
The
Company begins capitalization of qualifying costs when both the preliminary project stage is completed and management has authorized
further funding for the completion of the project. Costs incurred during the preliminary project stage along with post implementation
stages of internal-use computer software are expensed as incurred. The Company also capitalizes costs related to specific upgrades and
enhancements when it is probable the expenditures will result in additional functionality. Capitalized development costs are classified
as “Property and equipment, net” in the Consolidated Balance Sheets and are depreciated over the estimated useful life of the
software, which is generally five years.
Goodwill
The
excess of purchase price over the fair value of identifiable net assets acquired in business combinations is recorded as goodwill. As
of September 30, 2023, all the Company’s goodwill relates to the acquisition of Scendia Biologics, LLC (“Scendia”)
(see Note 4). Goodwill has an indefinite useful life and is not amortized. Goodwill is tested annually as of December 31 for impairment,
or more frequently if circumstances indicate impairment may have occurred. The Company may first perform a qualitative assessment to
determine if it is more likely than not that the fair value of the reporting unit is less than the respective carrying value. If it is
determined that it is more likely than not that a reporting unit’s fair value is less than its carrying value, then the Company
will determine the fair value of the reporting unit and record an impairment charge for the difference between fair value and carrying
value (not to exceed the carrying amount of goodwill). No impairment was recorded during the nine months ended September 30, 2023.
Intangible
Assets
Intangible
assets are stated at cost of acquisition less accumulated amortization and impairment loss, if any. Cost of acquisition includes the
purchase price and any cost directly attributable to bringing the asset to its working condition for the intended use. The Company amortizes
its finite-lived intangible assets on a straight-line basis over the estimated useful life of the respective assets which is generally
the life of the related patents or licenses, seven years for customer relationships and five years for assembled workforces. See Note
6 for more information on intangible assets.
Impairment
of Long-Lived Assets
Long-lived
assets, including certain identifiable intangibles held and to be used by the Company, are reviewed for impairment whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The Company continuously evaluates
the recoverability of its long-lived assets based on estimated future cash flows and the estimated liquidation value of such long-lived
assets and provides for impairment if such undiscounted cash flows are insufficient to recover the carrying amount of the long-lived
assets. If impairment exists, an adjustment is made to write the asset down to its fair value, and a loss is recorded as the difference
between the carrying value and fair value. Fair values are determined based on quoted market values, undiscounted cash flows or internal
and external appraisals, as applicable. Assets to be disposed of are carried at the lower of carrying value or estimated fair value less
cost to sell. No impairment was recorded during the nine months ended September 30, 2023 and 2022.
Investments
in Equity Securities
The
Company’s equity investments consist of nonmarketable equity securities in privately held companies without readily determinable
fair values. Unless accounted for under the equity method of accounting, the investments are reported at cost minus impairment, if any,
plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the
same issuer.
The
Company applies the equity method of accounting to investments when it has significant influence, but not controlling interest, in the
investee. Judgment regarding the level of influence over each equity method investment includes considering key factors such as ownership
interest, representation on the board of directors, participation in policy-making decisions and material intercompany transactions.
The Company’s proportionate share of the net income (loss) resulting from these investments is reported under the line item captioned
“Share of losses from equity method investment” in the Company’s Consolidated Statements of Operations. The Company’s
equity method investment is adjusted each period for the Company’s share of the investee’s income or loss and dividend paid,
if any. The Company classifies distributions received from its equity method investment using the cumulative earnings approach in the
Company’s Consolidated Statements of Cash Flows. As a result of the Precision Healing merger in April 2022 (see Note 3), the
Company did not have any investments which are recorded applying the equity method of accounting as of September 30, 2023.
The
Company has reviewed the carrying value of its investments and has determined there was no impairment or observable price changes as
of and for the nine months ended September 30, 2023 or 2022.
Fair
Value Measurement
As
defined in ASC Topic 820, Fair Value Measurement (“ASC 820”), fair value is the price that would be received to sell an asset
or paid to transfer a liability in an orderly transaction between market participants at the measurement date (exit price). The Company
utilizes market data or assumptions that market participants would use in pricing the asset or liability, including assumptions about
risk and the risks inherent in the inputs to the valuation technique. These inputs can be readily observable, market corroborated, or
generally unobservable. ASC 820 establishes a fair value hierarchy that prioritizes the inputs used to measure fair value. The hierarchy
gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurement) and
the lowest priority to unobservable inputs (Level 3 measurement). This fair value measurement framework applies at both initial and subsequent
measurement.
The
three levels of the fair value hierarchy defined by ASC 820 are as follows:
Level
1 – Quoted prices are available in active markets for identical assets or liabilities as of the reporting date. Active markets
are those in which transactions for the asset or liability occur in sufficient frequency and volume to provide pricing information on
an ongoing basis. Level 1 primarily consists of financial instruments such as exchange-traded derivatives, marketable securities and
listed equities.
Level
2 – Pricing inputs are other than quoted prices in active markets included in Level 1, which are either directly or indirectly
observable as of the reported date. Level 2 includes those financial instruments that are valued using models or other valuation methodologies.
These models are primarily industry-standard models that consider various assumptions, including quoted forward prices for commodities,
time value, volatility factors, and current market and contractual prices for the underlying instruments, as well as other relevant economic
measures. Substantially all these assumptions are observable in the marketplace throughout the full term of the instrument, can be derived
from observable data or are supported by observable levels at which transactions are executed in the marketplace. Instruments in this
category generally include nonexchange-traded derivatives such as commodity swaps, interest rate swaps, options and collars.
Level
3 – Pricing inputs include significant inputs that are generally less observable from objective sources. These inputs may be used
with internally developed methodologies that result in management’s best estimate of fair value.
The
carrying amounts of cash, accounts receivable, accounts payable and accrued expenses, other than acquisition-related accrued expenses,
approximate fair value because of the short-term nature of these instruments. The fair value of acquisition-related accrued expenses is categorized
as Level 2 of the fair value hierarchy. The value of these instruments has been estimated using discounted cash flow analysis based on
the Company’s incremental borrowing rate. The carrying value of the Company’s debt, which has
variable interest rates determined each month, approximates fair value based on instruments with similar terms (Level 2 inputs). The
fair value of the contingent earnout consideration and the acquisition date fair value of goodwill
and intangibles related to the acquisitions discussed in Notes 3, 4 and 5 are based on Level 3 inputs.
Liabilities
for contingent consideration are measured at fair value each reporting period, with the acquisition-date fair value included as part
of the consideration transferred. Subsequent changes in fair value are reported under the line item captioned “Change in fair value
of earnout liabilities” in the Company’s Consolidated Statements of Operations. The current year changes in fair value of earnout liabilities below are
as a result of a decrease in the estimated fair value of the earnout liabilities established at the time of the Company’s Precision Healing and
Scendia acquisitions. The following table sets forth a summary
of the changes in fair value for the Level 3 contingent earnout consideration.
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
Income
Taxes
Income
taxes are accounted for under the asset and liability method, whereby deferred income taxes are recorded for temporary differences between
financial statement carrying amounts and the tax basis of assets and liabilities. Deferred tax assets and liabilities reflect the tax
rates expected to be in effect for the years in which the differences are expected to reverse. A valuation allowance is provided if it
is more likely than not that some or all the deferred tax asset will not be realized.
Stock-based
Compensation
The
Company accounts for stock-based compensation to employees and nonemployees in accordance with Accounting Standards Update (“ASU”)
2018-07, Compensation – Stock Compensation (Topic 718). Stock-based compensation is measured at the grant date, based on the fair
value of the award, and is recognized as expense over the stipulated vesting period, if any. The Company estimates the fair value of
stock-based payments using the Black-Scholes option-pricing model for common stock options and warrants, and the closing price of the
Company’s common stock for grants of common stock, including restricted stock awards.
Research
and Development Costs
Research
and development (“R&D”) expenses consist of personnel-related expenses, including salaries and benefits for all personnel
directly engaged in R&D activities, contracted services, materials, prototype expenses and allocated overhead which is comprised
of lease expense and other facilities-related costs. R&D expenses include costs related to enhancements to the Company’s currently
available products and additional investments in the product, services and technologies development pipeline. The Company expenses R&D
costs as incurred.
Recently
Adopted Accounting Pronouncements
In
June 2016, the Financial Accounting Standards Board issued ASU 2016-13, Financial Instruments - Credit Losses (Topic 326). This update
amends the impairment model by requiring entities to use a forward-looking approach based on expected losses to estimate credit losses
for most financial assets and certain other instruments that are not measured at fair value through net income. The Company adopted the
new guidance effective January 1, 2023. The adoption did not have a material impact on the Company’s consolidated financial position,
results of operations or cash flows.
Recently
Issued Accounting Pronouncements
There
are no recently issued accounting pronouncements that have not yet been adopted that are expected to have a material effect on the Company’s
consolidated financial condition, results of operations or cash flows.
NOTE
3 – PRECISION HEALING MERGER
In
April 2022, the Company entered into a merger agreement by and among the Company, United Wound and Skin Solutions, LLC, a Delaware limited
liability company and wholly owned subsidiary of the Company, Precision Healing, PH Merger Sub I, Inc., a Delaware corporation, PH Merger
Sub II, LLC, a Delaware limited liability company, and Furneaux Capital Holdco, LLC (d/b/a BlueIO), solely in its capacity as the representative
of the securityholders of Precision Healing. On April 4, 2022 (the “Closing Date”), the merger parties closed the transactions
contemplated by the merger agreement and Precision Healing became a wholly owned subsidiary of the Company.
Precision
Healing is developing a diagnostic imager and lateral flow assay for assessing a patient’s wound and skin conditions. This comprehensive
skin and wound assessment technology is designed to quantify biochemical markers to determine the trajectory of a wound’s condition
to enable better diagnosis and treatment protocol. To date, Precision Healing has not generated revenues.
Pursuant
to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock, other than the Company, were entitled
to receive closing consideration, consisting of $125,966 in cash, which was paid to stockholders who were not accredited investors, 165,738
shares of the Company’s common stock, which was paid only to accredited investors, and the payment in cash of approximately $0.6
million of transaction expenses of Precision Healing. The Company recorded the issuance of the 165,738 shares to accredited investors
and cash payments to nonaccredited investors based on the closing price per share of the Company’s common stock on the Closing
Date, which was $30.75.
On
the Closing Date, the outstanding Precision Healing options previously granted under the Precision Healing Inc. 2020 Stock Option and
Grant Plan (the “Precision Healing Plan”) converted, pursuant to their terms, into options to acquire an aggregate of 144,191
shares of Company common stock with a weighted average exercise price of $10.71 per share. These options expire between August 2030 and
April 2031. In addition, outstanding and unexercised Precision Healing warrants converted into rights to receive warrants to purchase
(i) 4,424 shares of Company common stock with an initial exercise price of $7.32 per share and an expiration date of April 22, 2031,
and (ii) 12,301 shares of the Company’s common stock with an initial exercise price of $12.05 per share and an expiration date
of August 10, 2030.
Pursuant
to the merger agreement, the Company assumed sponsorship of the Precision Healing Plan, effective as of the Closing Date, as well as
the outstanding awards granted thereunder, the award agreements evidencing the grants of such awards and the remaining shares available
under the Precision Healing Plan, in each case adjusted in the manner set forth in the merger agreement. Concurrent with the assumption
of the Precision Healing Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC Topic 805, Business Combinations (“ASC 805”). The earnout consideration is payable in cash or, at the Company’s
election, is payable to accredited investors in shares of Company common stock at a price per share equal to the greater of (i) $27.13
or (ii) the average closing price of Company common stock for the 20 trading days prior to the date such earnout consideration is due
and payable. Pursuant to the merger agreement, a minimum percentage of the earnout consideration may be required to be issued to accredited
investors in shares of Company common stock for tax purposes. The amount and composition of the portion of earnout consideration payable
is subject to adjustment and offsets as set forth in the merger agreement.
As
the contingent earnout payments are not subject to any specific individual performance by the shareholders, the contingent shares are
not subject to ASC Topic 718, Compensation – Stock Compensation (“ASC 718”). Further, as the contingent consideration
was negotiated as part of the transfer of assets, the obligation was measured at fair value and included in the total purchase consideration
transferred. Additionally, the contingent earnout payments meet the criteria under ASC Topic 480, Distinguishing Liabilities from Equity
(“ASC 480”) as the monetary value of the shares to be issued is predominantly based on the exercise contingency (i.e., revenue
targets). Accordingly, the contingent consideration is classified as a liability at its estimated fair value at each reporting period
with the subsequent change in fair value recognized as a gain or loss in accordance with ASC 480.
The
total purchase consideration as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity
Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 165,738 | | |
$ | 5,096,444 | |
Fair value of assumed options | |
| 144,191 | | |
| 4,109,750 | |
Fair value of assumed warrants | |
| 16,725 | | |
| 502,895 | |
Cash paid to nonaccredited investors | |
| | | |
| 125,370 | |
Cash paid for fractional shares | |
| | | |
| 596 | |
Carrying value of equity method investment in Precision Healing | |
| | | |
| 1,803,440 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,882,151 | |
Direct transaction costs | |
| | | |
| 1,061,137 | |
Total purchase consideration | |
| | | |
$ | 16,581,783 | |
Based
on guidance provided by ASC 805, the Company recorded the Precision Healing merger as an asset acquisition due to the determination that
substantially all the fair value of the assets acquired was concentrated in a group of similar identifiable assets. The Company believes
the “substantially all” criterion was met with respect to the acquired intellectual property based on the Company’s
valuation models. These models assigned value to the acquired intellectual property based on estimated future cash flows. Accordingly,
the Company accounted for the merger as an asset acquisition.
The
purchase consideration, plus transaction costs, was allocated to the individual assets according to their fair values as a percentage
of the total fair value of the assets purchased, with no goodwill recognized. Based on the estimated fair value of the gross assets acquired,
the total fair value of the net assets acquired was primarily attributable to, and classified as, finite-lived intellectual property
and assembled workforce in the second quarter of 2022. The total purchase consideration was allocated based on the relative estimated
fair value of such assets as follows:
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 32,202 | |
Net working capital (excluding cash) | |
| (308,049 | ) |
Noncontrolling interest in Sanara Biologics, LLC | |
| | |
Customer relationships | |
| | |
Fixed assets, net | |
| 9,228 | |
Deferred tax assets | |
| 278,661 | |
Intellectual property | |
| 20,325,469 | |
Assembled workforce | |
| 664,839 | |
Deferred tax liabilities | |
| (4,420,567 | ) |
Goodwill | |
| | |
Net assets acquired | |
$ | 16,581,783 | |
NOTE
4 – SCENDIA PURCHASE AGREEMENT
In
July 2022, the Company entered into a membership interest purchase agreement by and among the Company, Scendia, a Delaware limited liability
company, and Ryan Phillips (“Phillips”) pursuant to which, and in accordance with the terms and conditions set forth therein,
the Company acquired 100% of the issued and outstanding membership interests in Scendia from Phillips.
Scendia
provides clinicians and surgeons with a full line of regenerative and orthobiologic technologies for their patients through certain customer
accounts. Beginning in early 2022, the Company began co-promoting certain products with Scendia, including: (i) TEXAGEN Amniotic Membrane
Allograft, (ii) BiFORM Bioactive Moldable Matrix, (iii) ACTIGEN Verified Inductive Bone Matrix and (iv) ALLOCYTE Advanced Cellular Bone
Matrix. Prior to the acquisition, Scendia owned 50% of the issued and outstanding membership interests in Sanara Biologics, LLC (“Sanara
Biologics”), and the Company owned the remaining 50% of the membership interests. As a result of the acquisition, the Company indirectly
acquired all the interests in Sanara Biologics, such that the Company now holds 100% of the issued and outstanding equity interests in
Sanara Biologics.
Pursuant
to the purchase agreement, Phillips was entitled to receive closing consideration consisting of (i) approximately $1.6 million of cash,
subject to certain adjustments, and (ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing,
the Company withheld 94,798 shares of common stock with an agreed upon value of $1.95 million (the “Indemnity Holdback Shares”),
which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’ indemnification
obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023.
As
the contingent earnout payments are not subject to any specific individual performance by Phillips, the contingent shares are not subject
to ASC 718. Further, as the contingent consideration was negotiated as part of the transfer of assets, the obligation was measured at
fair value and included in the total purchase consideration transferred. Additionally, the contingent earnout payments meet the criteria
under ASC 480, as the monetary value of the shares to be issued is predominantly based on the exercise contingency (i.e., revenue targets).
Accordingly, the contingent consideration is classified as a liability at its estimated fair value at each reporting period with the
subsequent change in fair value recognized as a gain or loss in accordance with ASC 480.
The
total purchase consideration, subject to typical post-closing adjustments, as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 291,686 | | |
$ | 6,032,066 | |
Cash consideration | |
| | | |
| 1,562,668 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,000,000 | |
Total purchase consideration | |
| | | |
$ | 10,594,734 | |
Based
on guidance provided by ASC 805, the Company recorded the Scendia acquisition as a business combination. The purchase consideration was
allocated to the individual assets according to their fair values as a percentage of the total fair value of the net assets purchased.
The excess of the purchase consideration over the net assets purchased was recorded as goodwill. The total purchase consideration was
allocated as follows:
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 201,406 | |
Net working capital (excluding cash) | |
| 1,294,499 | |
Fixed assets, net | |
| 42,300 | |
Noncontrolling interest in Sanara Biologics, LLC | |
| 2,638 | |
Customer relationships | |
| 7,155,000 | |
Deferred tax liabilities | |
| (1,702,890 | ) |
Goodwill | |
| 3,601,781 | |
Net assets acquired | |
$ | 10,594,734 | |
The
goodwill acquired consists of expected synergies from the acquisition to the Company’s overall corporate strategy. The Company
does not expect any of the goodwill to be deductible for income tax purposes. The Company incurred acquisition costs of approximately
$187,000 in 2022, which is included in “Selling, general and administrative expenses” in the accompanying Consolidated Statements
of Operations.
NOTE
5 – APPLIED ASSET PURCHASE
On
August 1, 2023, the Company entered into an Asset Purchase Agreement (the “Applied Purchase Agreement”) by and among the
Company, as guarantor, Sanara MedTech Applied Technologies, LLC, a Texas limited liability company and wholly owned subsidiary of
the Company (“SMAT”), The Hymed Group Corporation, a Delaware corporation (“Hymed”), Applied Nutritionals,
LLC, a Delaware limited liability company (“Applied”, and together with Hymed, the “Sellers”), and Dr.
George D. Petito (the “Owner”), pursuant to which SMAT acquired certain assets of the Sellers and the Owner, including,
among others, the Sellers’ and Owner’s inventory, intellectual property, manufacturing and related equipment, goodwill,
rights and claims, other than certain excluded assets, all as more specifically set forth in the Applied Purchase Agreement
(collectively, the “Applied Purchased Assets”), and assumed certain Assumed Liabilities (as defined in the Applied
Purchase Agreement), upon the terms and subject to the conditions set forth in the Applied Purchase Agreement (such transaction, the
“Applied Asset Purchase”). The Applied Purchased Assets include the underlying intellectual property of, as well as the
rights to manufacture and sell, CellerateRX Surgical Activated Collagen (Powder and Gel) (“CellerateRX Surgical”) and
HYCOL Hydrolyzed Collagen (Powder and Gel) (“HYCOL”) products for human wound care use.
The
Applied Purchased Assets were purchased for an initial aggregate purchase price of $15.25 million, consisting of (i) $9.75 million in
cash (the “Cash Closing Consideration”), (ii) 73,809 shares of the Company’s common stock (the “Stock Closing
Consideration”) with an agreed upon value of $3.0 million and (iii) $2.5 million in cash (the “Installment Payments”),
to be paid in four equal installments on each of the next four anniversaries of the closing of the Applied Asset Purchase (the “Closing”).
Prior
to the Closing, the Company licensed certain of its products from Applied through a sublicense agreement (the “Sublicense Agreement”)
with CGI Cellerate RX, LLC (“CGI Cellerate RX”), a related party (see Note 13 for additional information regarding transactions with related parties). Pursuant
to the Sublicense Agreement, the Company has an exclusive, world-wide sublicense to distribute CellerateRX Surgical and HYCOL products
into the surgical and wound care markets. In connection with the Applied Asset Purchase, Applied assigned its license agreement with
CGI Cellerate RX to SMAT. Since the Closing of the Applied Asset Purchase, Sanara indirectly makes intercompany royalty payments to SMAT
at the same rate as set forth in the Sublicense Agreement. Effective August 1, 2023, these intercompany royalty payments and the offsetting cost of goods sold are eliminated
on a consolidated basis.
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive up to an additional $10.0 million (the “Applied Earnout”), which is payable to the
Sellers in cash, upon the achievement of certain performance thresholds relating to SMAT’s collections from net sales of a collagen-based
product currently under development. Upon expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned
the entirety of the Applied Earnout, SMAT shall pay the Sellers a pro-rata amount of the Applied Earnout based on collections from net
sales of the product, with such amount to be due credited against any Applied Earnout payments already made by SMAT (the “True-Up
Payment”). The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already made by SMAT, may be earned
at any point in the future, including after the True-Up Payment is made.
In
connection with the Applied Asset Purchase and pursuant to the Applied Purchase Agreement, effective August 1, 2023, the Company entered
into a professional services agreement (the “Petito Services Agreement”) with the Owner, pursuant to which the Owner, as
an independent contractor, agreed to provide certain services to the Company, including, among other things, assisting with the development
of products already in development and assisting with research, development, formulation, invention and manufacturing of any future products
(the “Petito Services”). As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of
$12,000 per month during the term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual
collections from net sales of certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment
equal to five percent (5%) for the first $50.0 million in aggregate collections from net sales of certain future products and a royalty
payment of two and one-half percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding
$50.0 million but up to $100.0 million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted
by the Company and (v) $1.0 million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect
to the incentive payments described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
The
Petito Services Agreement has an initial term of three years and is subject to automatic successive one-month renewals unless earlier
terminated in accordance with its terms. The Petito Services Agreement may be terminated upon the Owner’s death or disability or
by the Company or the Owner “For Cause” (as defined in the Petito Services Agreement); provided, however, that the base salary
described in (i) of the foregoing paragraph shall survive termination through the three-year initial term and the royalty payments and
incentive payments described in (ii)-(v) of the foregoing paragraph shall survive termination of the Petito Services Agreement.
As
the contingent consideration was negotiated as part of the transfer of assets, the contingent obligations were
measured at fair value and included in the total purchase consideration transferred. Accordingly, the contingent consideration
is classified as a liability at its estimated fair value at each reporting period with the subsequent change in fair value recognized
as a gain or loss.
The
total purchase consideration for the Applied Asset Purchase as determined by the Company was as follows:
SCHEDULE
OF PURCHASE CONSIDERATION
Consideration | |
Equity Shares | | |
Dollar Value | |
Cash Closing Consideration | |
| | | |
$ | 9,750,000 | |
Fair value of Stock Closing Consideration | |
| 73,809 | | |
| 3,089,645 | |
Fair value of Installment Payments | |
| | | |
| 2,040,808 | |
Cash paid for inventory | |
| | | |
| 30,007 | |
Fair value of Petito Services Agreement defined payments | |
| | | |
| 825,834 | |
Fair value of Petito Services Agreement contingent consideration | |
| | | |
| 893,000 | |
Direct transaction costs | |
| | | |
| 162,743 | |
Total purchase consideration | |
| | | |
$ | 16,792,037 | |
Based
on guidance provided by ASC 805, the Company recorded the Applied Asset Purchase as an asset acquisition due to the determination that
substantially all the fair value of the assets acquired was concentrated in a group of similar identifiable assets. The Company believes
the “substantially all” criterion was met with respect to the acquired intellectual property being the only significant asset
acquired. Accordingly, the Company accounted for the transaction as an asset acquisition.
The
purchase consideration, plus transaction costs, was allocated to the individual assets according to their fair values as a percentage
of the total fair value of the assets purchased, with no goodwill recognized. Based on the estimated fair value of the gross assets acquired,
the total fair value of the net assets acquired was primarily attributable to, and classified as, finite-lived intellectual property
in the third quarter of 2023. The total purchase consideration was allocated based on the relative estimated fair value of such assets
as follows:
SCHEDULE
OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Inventory | |
$ | 30,007 | |
Equipment | |
| 33,062 | |
Intellectual property | |
| 16,728,968 | |
Net assets acquired | |
$ | 16,792,037 | |
NOTE
6 – INTANGIBLE ASSETS
The
carrying values of the Company’s intangible assets were as follows for the periods presented:
SCHEDULE OF FINITE LIVED INTANGIBLE ASSETS
| |
September 30, 2023 | | |
December 31, 2022 | |
| |
| | |
Accumulated | | |
| | |
| | |
Accumulated | | |
| |
| |
Cost | | |
Amortization | | |
Net | | |
Cost | | |
Amortization | | |
Net | |
Amortizable Intangible Assets: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Product licenses | |
$ | 4,793,879 | | |
$ | (1,246,115 | ) | |
$ | 3,547,764 | | |
$ | 4,793,879 | | |
$ | (980,583 | ) | |
$ | 3,813,296 | |
Patents and other IP | |
| 38,664,548 | | |
| (2,598,220 | ) | |
| 36,066,328 | | |
| 21,935,580 | | |
| (1,492,057 | ) | |
| 20,443,523 | |
Customer relationships and other | |
| 7,947,332 | | |
| (1,569,958 | ) | |
| 6,377,374 | | |
| 7,947,332 | | |
| (694,171 | ) | |
| 7,253,161 | |
Total | |
$ | 51,405,759 | | |
$ | (5,414,293 | ) | |
$ | 45,991,466 | | |
$ | 34,676,791 | | |
$ | (3,166,811 | ) | |
$ | 31,509,980 | |
As
of September 30, 2023, the weighted-average amortization period for finite-lived intangible assets was 14.5 years. Amortization expense
related to intangible assets was $881,079 and $708,534 for the three months ended September 30, 2023 and 2022, respectively, and $2,247,482
and $1,256,097 for the nine months ended September 30, 2023 and 2022, respectively. The estimated remaining amortization expense as of
September 30, 2023 for finite-lived intangible assets is as follows:
SCHEDULE OF FUTURE AMORTIZATION EXPENSE
| |
| | |
Remainder of 2023 | |
$ | 974,018 | |
2024 | |
| 3,896,070 | |
2025 | |
| 3,896,070 | |
2026 | |
| 3,878,815 | |
2027 | |
| 3,764,962 | |
2028 | |
| 3,731,721 | |
Thereafter | |
| 25,849,810 | |
Total | |
$ | 45,991,466 | |
The
Company has reviewed the carrying value of intangible assets and has determined there was no impairment during either of the nine months
ended September 30, 2023 or 2022.
NOTE
7 – INVESTMENTS IN EQUITY SECURITIES
The
Company’s equity investments consist of nonmarketable equity securities in privately held companies without readily determinable
fair values. Unless accounted for under the equity method of accounting, the investments are reported at cost minus impairment, if any,
plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the
same issuer.
In
July 2020, the Company made a $500,000 long-term investment to purchase certain nonmarketable securities consisting of 7,142,857 Series
B-2 Preferred Shares of Direct Dermatology Inc. (“DirectDerm”), representing approximately 2.9% ownership of DirectDerm at
that time. Through this investment, the Company received exclusive rights to utilize DirectDerm’s technology in all acute and post-acute
care settings such as skilled nursing facilities, home health and wound clinics. The Company does not have the ability to exercise significant
influence over DirectDerm’s operating and financial activities. In 2021, the Company purchased an additional 3,571,430 shares of
DirectDerm’s Series B-2 Preferred for $250,000. In March 2022, the Company purchased an additional 3,571,429 shares of DirectDerm’s
Series B-2 Preferred for $250,000. The Company’s ownership of DirectDerm was approximately 8.1% as of September 30, 2023.
In
November 2020, the Company entered into agreements to purchase certain nonmarketable securities consisting of 150,000 shares of Series
A Convertible Preferred Stock (the “Series A Stock”) of Precision Healing for an aggregate purchase price of $600,000. The
Series A Stock was convertible into 150,000 shares of common stock of Precision Healing and had a senior liquidation preference relative
to the common shareholders. This initial investment represented approximately 12.6% ownership of Precision Healing’s outstanding
voting securities. In February 2021, the Company invested $600,000 to purchase 150,000 additional shares of Series A Stock which was
convertible into 150,000 shares of common stock of Precision Healing. This resulted in ownership of approximately 22.4% of Precision
Healing’s outstanding voting securities. With this level of significant influence, the Company transitioned to the equity method
of accounting for this investment. In June 2021, the Company invested $500,000 for 125,000 additional shares of Series A Stock, which
increased the Company’s ownership of Precision Healing’s outstanding voting securities to approximately 29.0%. In October
and December of 2021, 125,000 and 150,000 more shares of Series A Stock were purchased for $500,000 and $600,000, respectively.
As
discussed above, in April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became
a wholly owned subsidiary of the Company (see Note 3 for more information). As a result of the merger, the Company’s equity method
investment in Precision Healing ceased in April 2022. The Company recorded $379,633 in the nine months ended September 30, 2022 as its
share of the loss from this equity method investment for the period prior to acquisition.
In
June 2021, the Company invested $2,084,278 to purchase 278,587 Class A Preferred Shares (the “Pixalere Shares”) of Canada-based
Pixalere Healthcare Inc. (“Pixalere”). The Pixalere Shares are convertible into approximately 27.3% of the outstanding equity
of Pixalere. Pixalere provides a cloud-based wound care software tool that empowers nurses, specialists and administrators to deliver
better care for patients. In connection with the Company’s purchase of the Pixalere Shares, Pixalere granted Pixalere Healthcare
USA, LLC (“Pixalere USA”), a subsidiary of the Company, a royalty-free exclusive license to use the Pixalere software and
platform in the United States. In conjunction with the grant of the license, the Company issued Pixalere a 27.3% equity ownership interest
in Pixalere USA valued at $93,879.
The
Company has reviewed the characteristics of the Pixalere Shares in accordance with ASC Topic 323, Investments – Equity Method and
Joint Ventures. Due to the substantive liquidation preferences of the Pixalere Shares over Pixalere’s common stock, the Pixalere
Shares are not “in-substance” common stock, and therefore, the Company does not utilize the equity method of accounting for
this investment. In accordance with ASC Topic 321, Investments - Equity Securities, this investment was reported at cost as of September
30, 2023.
The
following summarizes the Company’s investments for the periods presented:
SCHEDULE
OF INVESTMENTS
| |
September
30, 2023 | | |
December
31, 2022 | |
| |
| Carrying
Amount | | |
| Economic
Interest | | |
| Carrying
Amount | | |
| Economic
Interest | |
Equity
Method Investment | |
| | | |
| | | |
| | | |
| | |
Precision
Healing Inc. | |
$ | - | | |
| - | % | |
$ | - | | |
| - | % |
| |
| | | |
| | | |
| | | |
| | |
Cost
Method Investments | |
| | | |
| | | |
| | | |
| | |
Direct
Dermatology, Inc. | |
| 1,000,000 | | |
| | | |
| 1,000,000 | | |
| | |
Pixalere
Healthcare Inc. | |
| 2,084,278 | | |
| | | |
| 2,084,278 | | |
| | |
Total
Cost Method Investments | |
| 3,084,278 | | |
| | | |
| 3,084,278 | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Total
Investments | |
$ | 3,084,278 | | |
| | | |
$ | 3,084,278 | | |
| | |
The
following summarizes the loss from the equity method investment reflected in the Consolidated Statements of Operations:
SCHEDULE OF LOSS FROM EQUITY METHOD INVESTMENT
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three
Months ended September 30, | | |
Nine
Months Ended September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Investment | |
| | |
| | |
| | |
| |
Precision
Healing Inc. | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
| |
| | | |
| | | |
| | | |
| | |
Total | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
Loss from equity method
investment | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
NOTE
8 – OPERATING LEASES
The
Company periodically enters operating lease contracts for office space and equipment. Arrangements are evaluated at inception to determine
whether such arrangements constitute a lease. Right of use assets (“ROU assets”) represent the right to use an underlying
asset for the lease term and lease liabilities represent the obligation to make lease payments arising from the lease. Operating lease
ROU assets and liabilities were recognized on the transition date based on the present value of lease payments over the respective lease
term, with the office space ROU asset adjusted for deferred rent liability.
The
Company has three material operating leases for office space. In March and September 2023, the Company amended its primary office lease
to obtain additional space, as well as extend the term. The leases have remaining lease terms of 87, 40 and 23 months as of September
30, 2023. For practical expediency, the Company has elected to not recognize ROU assets and lease liabilities related to short-term leases.
In
accordance with ASC Topic 842, Leases, the Company has recorded ROU assets of $2,094,188 and a related lease liability of $2,168,499
as of September 30, 2023. The Company recorded lease expense of $295,268 and $210,317 for the nine months ended September 30, 2023 and
2022, respectively, for its leased assets. Cash paid for amounts included in the measurement of operating lease liabilities was $264,291
and $210,897 for the nine months ended September 30, 2023 and 2022, respectively. The present value of the Company’s operating
lease liabilities as of September 30, 2023 is shown below.
Maturity
of Operating Lease Liabilities
SCHEDULE OF OPERATING LEASE LIABILITY
| |
September 30,
2023 | |
Remainder of 2023 | |
$ | 116,285 | |
2024 | |
| 505,017 | |
2025 | |
| 532,053 | |
2026 | |
| 379,529 | |
2027 | |
| 297,947 | |
2028 | |
| 295,689 | |
Thereafter | |
| 604,049 | |
Total lease payments | |
| 2,730,569 | |
Less imputed interest | |
| (562,070 | ) |
Present Value of Lease Liabilities | |
$ | 2,168,499 | |
| |
| | |
Operating lease liabilities – current | |
| 322,206 | |
Operating lease liabilities – long-term | |
| 1,846,293 | |
As
of September 30, 2023, the Company’s operating leases had a weighted average remaining lease term of 6.0 years and a weighted average
discount rate of 7.59%.
NOTE
9 – DEBT AND CREDIT FACILITIES
In
connection with the entry into the Applied Purchase Agreement, on August 1, 2023, SMAT, as borrower, and the Company, as guarantor, entered
into a loan agreement (the “Loan Agreement”) with Cadence Bank (the “Bank”) providing for, among other things,
an advancing term loan in the aggregate principal amount of $12.0 million (the “Term Loan”), which was evidenced by an advancing
promissory note. Pursuant to the Loan Agreement, the Bank agreed to make, at any time and from time to time prior to February 1, 2024,
one or more advances to SMAT.
The
proceeds of the advances under the Loan Agreement will be used for working capital and for purposes of financing up to one hundred percent
(100%) of the Cash Closing Consideration and Installment Payments for the Applied Asset Purchase and related fees and expenses, including
any subsequent payments that may be due to the Sellers after the Closing. On August 1, 2023, the Bank, at the request of SMAT, made an
advance for $9.75 million. The proceeds from the advance were used to fund the Cash Closing Consideration for the Applied Asset Purchase.
Advances
under the Term Loan will begin amortizing in monthly installments commencing on August 5, 2024. All remaining unpaid balances under the
Term Loan are due and payable in full on August 1, 2028 (the “Maturity Date”). SMAT may prepay amounts due under the Term
Loan. All accrued but unpaid interest on the unpaid principal balance of outstanding advances is due and payable monthly, beginning on
September 5, 2023 and continuing monthly on the fifth day of each month thereafter until the Maturity Date. The unpaid principal balance
of outstanding advances bears interest, subject to certain conditions, at the lesser of the Maximum Rate (as defined in the Loan Agreement)
or the Base Rate, which is for any day, a rate per annum equal to the term secured overnight financing rate (Term SOFR) (as administered
by the Federal Reserve Bank of New York) for a one-month tenor in effect on such day plus three percent (3.0%).
The
obligations of SMAT under the Loan Agreement and the other loan documents delivered in connection therewith are guaranteed by the Company
and are secured by a first priority security interest in substantially all of the existing and future assets of SMAT.
The
Loan Agreement contains customary representations and warranties and certain covenants that limit (subject to certain exceptions) the
ability of SMAT and the Company to, among other things, (i) create, assume or guarantee certain liabilities, (ii) create, assume or suffer
liens securing indebtedness, (iii) make or permit loans and advances, (iv) acquire any assets outside the ordinary course of business,
(v) consolidate, merge or sell all or a material part of its assets, (vi) pay dividends or other distributions on, or redeem or repurchase,
interest in an obligor, including the Company, as guarantor (vii) cease, suspend or materially curtail business operations or (viii)
engage in certain affiliate transactions. In addition, the Loan Agreement contains financial covenants that require SMAT to maintain
(i) a minimum Debt Services Coverage Ratio of 1.2 to 1.0 as of the last day of each applicable fiscal quarter and (ii) a maximum Cash
Flow Leverage Ratio of not more than (a) 4.5 to 1.0 as of the last day of the fiscal quarter ending on September 30, 2023, (b) 4.0 to
1.0 as of the last day of each fiscal quarter ending on December 31, 2023 and March 31, 2024, (c) 3.5 to 1.0 as of the last day of each
fiscal quarter ending June 30, 2024 and September 30, 2024 and (d) 3.0 to 1.0 as of the last day of each fiscal quarter thereafter. Pursuant
to the Loan Agreement, in the event that SMAT fails to comply with the financial covenants described above, the Company is required to
contribute cash to SMAT in an amount equal to the amount required to satisfy the financial covenants. During the three months ended September 30, 2023, the Company contributed an immaterial amount of cash to SMAT in order to permit SMAT
to be in compliance with the financial covenants under the Loan Agreement. The Company was in compliance with
the financial covenants under the Loan Agreement as of September 30, 2023.
The
Loan Agreement also contains customary events of default. If such an event of default occurs, the Bank would be entitled to take various
actions, including the acceleration of amounts due under the Loan Agreement and actions permitted to be taken by a secured creditor.
The
table below presents the components of outstanding debt for the periods presented:
SCHEDULE
OF LONG-TERM DEBT
| |
September 30, 2023 | | |
December 31, 2022 | |
Term Loan | |
$ | 9,750,000 | | |
$ | - | |
Total debt | |
| 9,750,000 | | |
| - | |
Less: debt issuance costs, net of accumulated amortization of $2,055 and zero | |
| (59,603 | ) | |
| - | |
Long-term debt | |
| 9,690,397 | | |
| - | |
Less: current portion of debt | |
| 232,143 | | |
| - | |
Long-term debt, net of current portion | |
$ | 9,458,254 | | |
$ | - | |
As
of September 30, 2023, the interest rate on the advance under the Term Loan was 8.3%.
The
table below presents the aggregate maturities of the Company’s outstanding debt as of September 30, 2023:
SCHEDULE
OF MATURITIES OUTSTANDING DEBT
Year | |
Total | |
Remainder of 2023 | |
$ | - | |
2024 | |
| 580,357 | |
2025 | |
| 1,625,000 | |
2026 | |
| 1,950,000 | |
2027 | |
| 1,950,000 | |
2028 | |
| 3,644,643 | |
Thereafter | |
| - | |
Total debt | |
$ | 9,750,000 | |
In
connection with the Term Loan, the Company incurred $61,658
in debt issuance costs during the three months ended September 30, 2023. Debt issuance costs are amortized to “Interest
expense and other” on the Consolidated Statement of Operations over the life of the debt to which they pertain. The total
unamortized debt issuance costs were $59,603
and zero
as of September 30, 2023 and December 31, 2022, respectively. Debt issuance costs are included in “Long-term debt, net of
current portion” on the Consolidated Balance Sheets. Amortization expense related to debt issuance costs was $2,055
and zero
for the three and nine months ended September 30, 2023 and 2022, respectively.
NOTE
10 – COMMITMENTS AND CONTINGENCIES
License
Agreements and Royalties
CellerateRX
Surgical Activated Collagen
In
August 2018, the Company entered into the Sublicense Agreement with CGI Cellerate RX to distribute CellerateRX Surgical and HYCOL
products into the surgical and wound care markets. Pursuant to the Sublicense Agreement, the Company pays royalties of 3-5% of
annual collected net sales of CellerateRX Surgical and HYCOL. As amended in January 2021, the term of the sublicense extends through
May 2050, with automatic successive year-to-year renewal terms thereafter so long as the Company’s Net Sales (as defined in
the Sublicense Agreement) each year are equal to or in excess of $1,000,000. If the Company’s Net Sales fall below $1,000,000
for any year after the initial expiration date, CGI Cellerate RX will have the right to terminate the Sublicense Agreement upon
written notice.
Under
this agreement, royalty expense, which is recorded in “Cost of goods sold” in the accompanying Consolidated Statements
of Operations, totaled a benefit of $9,209 for
the three months ended September 30, 2023 due to the reversal of an accrual and $432,809
of expense for the three months ended September 30, 2022, respectively. Royalty expense totaled $1,060,035 and
$1,245,775 for
the nine months ended September 30, 2023 and 2022, respectively. Sales of CellerateRX Surgical comprised the substantial majority of
the Company’s sales during the three and nine months ended September 30, 2023 and 2022.
As
discussed further in Note 5, on August 1, 2023, the Company purchased certain assets from Applied, including the underlying
intellectual property of, as well as the rights to manufacture and sell, CellerateRX Surgical and HYCOL products. In connection with
the Applied Asset Purchase, Applied assigned its license agreement with CGI Cellerate RX to SMAT. Since the Closing, Sanara
indirectly makes intercompany royalty payments to SMAT at the same rate as set forth in the Sublicense Agreement. Effective August 1, 2023, these intercompany royalty payments and the offsetting cost of goods sold are eliminated
on a consolidated basis.
BIAKŌS
Antimicrobial Wound Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser
In
July 2019, the Company executed a license agreement with Rochal Industries, LLC (“Rochal”), a related party, pursuant to
which the Company acquired an exclusive world-wide license to market, sell and further develop antimicrobial products for the prevention
and treatment of microbes on the human body utilizing certain Rochal patents and pending patent applications (the “BIAKŌS
License Agreement”). Currently, the products covered by the BIAKŌS License Agreement are BIAKŌS Antimicrobial Wound
Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser. Both products are 510(k) cleared.
Future
commitments under the terms of the BIAKŌS License Agreement include:
| ● | The
Company pays Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to Rochal
was $120,000 for 2022 and will increase by $10,000 each subsequent calendar year up to a
maximum amount of $150,000. |
| ● | The
Company pays additional royalty annually based on specific net profit targets from sales
of the licensed products, subject to a maximum of $1,000,000 during any calendar year. |
Unless
previously terminated by the parties, the BIAKŌS License Agreement expires with the related patents in December 2031.
Under
this agreement, royalty expense, which is recorded in “Cost of goods sold” in the accompanying Consolidated Statements of
Operations, was $32,499 and $30,000 for the three months ended September 30, 2023 and 2022, respectively. For the nine months ended September
30, 2023 and 2022, royalty expense was $97,499 and $90,000, respectively. The Company’s Executive Chairman is a director of Rochal,
and indirectly a significant shareholder of Rochal, and through the potential exercise of warrants, a majority shareholder of Rochal.
Another one of the Company’s directors is also a director and significant shareholder of Rochal.
CuraShield
Antimicrobial Barrier Film and No Sting Skin Protectant
In
October 2019, the Company executed a license agreement with Rochal pursuant to which the Company acquired an exclusive world-wide license
to market, sell and further develop certain antimicrobial barrier film and skin protectant products for use in the human health care
market utilizing certain Rochal patents and pending patent applications (the “ABF License Agreement”). Currently, the products
covered by the ABF License Agreement are CuraShield Antimicrobial Barrier Film and a no sting skin protectant product.
Future
commitments under the terms of the ABF License Agreement include:
| ● | The
Company will pay Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to
Rochal will be $50,000 beginning with the first full calendar year following the year in
which first commercial sales of the products occur. The annual minimum royalty will increase
by 10% each subsequent calendar year up to a maximum amount of $75,000. |
| ● | The
Company will pay additional royalties annually based on specific net profit targets from
sales of the licensed products, subject to a maximum of $500,000 during any calendar year. |
Unless
previously terminated or extended by the parties, the ABF License Agreement will terminate upon expiration of the last U.S. patent in
October 2033. No commercial sales or royalties had been recognized under this agreement as of September 30, 2023.
Debrider
License Agreement
In
May 2020, the Company executed a product license agreement with Rochal, pursuant to which the Company acquired an exclusive world-wide
license to market, sell and further develop a debrider for human medical use to enhance skin condition or treat or relieve skin disorders,
excluding uses primarily for beauty, cosmetic, or toiletry purposes (the “Debrider License Agreement”).
Future
commitments under the terms of the Debrider License Agreement include:
| ● | Upon
FDA clearance of the licensed products, the Company will pay Rochal $500,000 in cash and
an additional $1,000,000, which at the Company’s option may be paid in any combination
of cash and its common stock. |
| ● | The
Company will pay Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to
Rochal will be $100,000 beginning with the first full calendar year following the year in
which first commercial sales of the licensed products occur and increase by 10% each subsequent
calendar year up to a maximum amount of $150,000. |
| ● | The
Company will pay additional royalty annually based on specific net profit targets from sales
of the licensed products, subject to a maximum of $1,000,000 during any calendar year. |
Unless
previously terminated or extended by the parties, the Debrider License Agreement will expire in October 2034. No commercial sales or
royalties have been recognized under this agreement as of September 30, 2023.
Resorbable
Bone Hemostat
The
Company acquired a patent in 2009 for a resorbable bone hemostat and delivery system for orthopedic bone void fillers. In connection
with the patent acquisition, the Company entered into a royalty agreement to pay 8% of the Company’s net revenues, including royalty
revenues, generated from products that utilize the Company’s acquired patented bone hemostat and delivery system. This patent is
not part of the Company’s long-term strategic focus. The Company subsequently licensed the patent to a third party to market a
bone void filler product for which the Company receives a 2% royalty on product sales through the end of 2023, with annual minimum royalties
of $201,000. To date, royalty revenues received by the Company related to this licensing agreement have not exceeded the annual minimum
of $201,000 ($50,250 per quarter). Therefore, the Company’s annual royalty obligation has been $16,080 ($4,020 per quarter), with
the expense being reported in “Cost of goods sold” in the accompanying Consolidated Statements of Operations.
Rochal
Asset Acquisition
In
July 2021, the Company entered into an asset purchase agreement with Rochal effective July 1, 2021, pursuant to which the Company purchased
certain assets of Rochal. Pursuant to the asset purchase agreement, for the three-year period after the effective date, Rochal is entitled
to receive consideration for any new product relating to the business that is directly and primarily based on an invention conceived
and reduced to practice by a member or members of Rochal’s science team. For the three-year period after the effective date, Rochal
is also entitled to receive an amount in cash equal to twenty-five percent of the proceeds received for any Grant (as defined in the
asset purchase agreement) by either the Company or Rochal. In addition, the Company agreed to use commercially reasonable efforts to
perform Minimum Development Efforts (as defined in the asset purchase agreement) with respect to certain products under development,
which if obtained, will entitle the Company to intellectual property rights from Rochal in respect of such products.
Precision
Healing Merger Agreement
In
April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became a wholly owned
subsidiary of the Company. Pursuant to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock,
other than the Company, were entitled to receive closing consideration, consisting of $125,966 in cash consideration, which was paid
to stockholders who were not accredited investors, 165,738 shares of the Company’s common stock, which was paid only to accredited
investors, and the payment in cash of approximately $0.6 million of transaction expenses of Precision Healing. The Company recorded the
issuance of the 165,738 shares to accredited investors and cash payments to nonaccredited investors based on the closing price per share
of the Company’s common stock on April 4, 2022, which was $30.75.
Upon
the closing of the merger, the Precision Healing outstanding options previously granted under the Precision Healing Plan converted, pursuant
to their terms, into options to acquire an aggregate of 144,191 shares of Company common stock with a weighted average exercise price
of $10.71 per share. These options expire between August 2030 and April 2031. In addition, outstanding and unexercised Precision Healing
warrants converted into rights to receive warrants to purchase (i) 4,424 shares of Company common stock with an initial exercise price
of $7.32 per share and an expiration date of April 22, 2031, and (ii) 12,301 shares of the Company’s common stock with an initial
exercise price of $12.05 per share and an expiration date of August 10, 2030. Concurrent with the assumption of the Precision Healing
Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC 805. The earnout consideration is payable in cash or, at the Company’s election, is payable to accredited investors
in shares of Company common stock at a price per share equal to the greater of (i) $27.13 or (ii) the average closing price of Company
common stock for the 20 trading days prior to the date such earnout consideration is due and payable. Pursuant to the merger agreement,
a minimum percentage of the earnout consideration may be required to be issued to accredited investors in shares of Company common stock
for tax purposes. The amount and composition of the portion of earnout consideration payable is subject to adjustment and offsets as
set forth in the merger agreement. See Note 3 for more information regarding the merger with Precision Healing.
Scendia
Purchase Agreement
In
July 2022, the Company closed the Scendia acquisition pursuant to which Scendia became a wholly owned subsidiary of the Company. Pursuant
to the purchase agreement, the aggregate consideration for the acquisition at closing was approximately $7.6 million, subject to customary
post-closing adjustments. The consideration consisted of (i) approximately $1.6 million of cash, subject to certain adjustments, and
(ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing, the Company withheld 94,798 Indemnity
Holdback Shares, which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’
indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023. The Company expects the second earnout payment to be made in the third quarter of 2024.
See Note 4 for more information regarding the acquisition of Scendia.
Applied
Asset Purchase
On
August 1, 2023, the Company closed the Applied Asset Purchase. The Applied Purchased Assets were purchased for an initial aggregate
purchase price of $15.25
million, consisting of (i) the Cash Closing Consideration , (ii) the Stock Closing Consideration and (iii) the Installment
Payments.
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive the Applied Earnout, which is payable to the Sellers in cash, upon the achievement of certain
performance thresholds relating to SMAT’s collections from net sales of a collagen-based product currently under development. Upon
expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned the entirety of the Applied Earnout,
SMAT shall pay the Sellers the True-Up Payment. The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already
made by SMAT, may be earned at any point in the future, including after the True-Up Payment is made.
In
connection with the Applied Asset Purchase and pursuant to the Applied Purchase Agreement, effective August 1, 2023, the Company entered
into the Petito Services Agreement with the Owner, pursuant to which the Owner, as an independent contractor, agreed to provide the Petito
Services. As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of $12,000 per month during the
term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual collections from net sales of
certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment equal to five percent (5%) for
the first $50.0 million in aggregate collections from net sales of certain future products and a royalty payment of two and one-half
percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding $50.0 million but up to $100.0
million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted by the Company and (v) $1.0
million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect to the incentive payments
described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
The
Petito Services Agreement has an initial term of three years and is subject to automatic successive one-month renewals unless earlier
terminated in accordance with its terms. The Petito Services Agreement may be terminated upon the Owner’s death or disability or
by the Company or the Owner “For Cause” (as defined in the Petito Services Agreement); provided, however, that the base salary
described in (i) of the foregoing paragraph shall survive termination through the three-year initial term and the royalty payments and
incentive payments described in (ii)-(v) of the foregoing paragraph shall survive termination of the Petito Services Agreement.
Other
Commitments
In
May 2019, the Company organized Sanara Pulsar, LLC (“Sanara Pulsar”), a Texas limited liability company, which was owned
60% by the Company’s wholly owned subsidiary Cellerate, LLC, and 40% owned by Wound Care Solutions, Limited (“WCS”),
an unaffiliated company registered in the United Kingdom. At the time of the formation of Sanara Pulsar, it and WCS, entered into a supply
agreement whereby Sanara Pulsar became the exclusive distributor in the United States of certain wound care products that utilize intellectual
property developed and owned by WCS. Pursuant to the operating agreement of Sanara Pulsar, in the event WCS’s annual Form K-l does
not allocate to WCS net income of at least $200,000 (the “Target Net Income”), the Company is required, within 30 days after
such determination, to pay WCS the amount of funds representing the difference between the Target Net Income and the actual amount of
net income shown on WCS’s Form K-1, as a distribution from Sanara Pulsar to WCS. For each of the years 2021 through 2024 the Target
Net Income was to increase by 10%. In April 2022, the Company paid WCS $220,000 related to the fiscal 2021 Form K-1 and in December 2022,
the Company accrued an additional payment of $242,000 related to the projected fiscal 2022 Form K-1. Sanara Pulsar, which had minimal
sales since its inception, was dissolved effective December 2022, and accordingly, there will be no additional payments made beyond the
accrued payment.
NOTE
11 – SHAREHOLDERS’ EQUITY
Common
Stock
At
the Company’s Annual Meeting of Shareholders held in July 2020, the Company approved the Restated 2014 Omnibus Long Term Incentive
Plan (the “LTIP Plan”) in which the Company’s directors, officers, employees and consultants are eligible to participate.
A total of 587,465 shares had been issued under the LTIP Plan and 1,412,535 were available for issuance as of September 30, 2023.
In
April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became a wholly owned
subsidiary of the Company. Pursuant to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock,
other than the Company, were entitled to receive closing consideration, consisting of $125,966 in cash consideration, which was paid
to stockholders who were not accredited investors, 165,738 shares of the Company’s common stock, which was paid only to accredited
investors, and the payment in cash of approximately $0.6 million of transaction expenses of Precision Healing. The Company recorded the
issuance of the 165,738 shares to accredited investors and cash payments to nonaccredited investors based on the closing price per share
of the Company’s common stock on April 4, 2022, which was $30.75.
Upon
the closing of the merger, the Precision Healing outstanding options previously granted under the Precision Healing Plan converted, pursuant
to their terms, into options to acquire an aggregate of 144,191 shares of Company common stock with a weighted average exercise price
of $10.71 per share. These options expire between August 2030 and April 2031. In addition, outstanding and unexercised Precision Healing
warrants converted into rights to receive warrants to purchase (i) 4,424 shares of Company common stock with an initial exercise price
of $7.32 per share and an expiration date of April 22, 2031, and (ii) 12,301 shares of the Company’s common stock with an initial
exercise price of $12.05 per share and an expiration date of August 10, 2030. Concurrent with the assumption of the Precision Healing
Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC 805. The earnout consideration is payable in cash or, at the Company’s election, is payable to accredited investors
in shares of Company common stock at a price per share equal to the greater of (i) $27.13 or (ii) the average closing price of Company
common stock for the 20 trading days prior to the date such earnout consideration is due and payable. Pursuant to the merger agreement,
a minimum percentage of the earnout consideration may be required to be issued to accredited investors in shares of Company common stock
for tax purposes. The amount and composition of the portion of earnout consideration payable is subject to adjustment and offsets as
set forth in the merger agreement. See Note 3 for more information regarding the merger with Precision Healing.
In
July 2022, the Company closed the Scendia acquisition pursuant to which Scendia became a wholly owned subsidiary of the Company. Pursuant
to the purchase agreement, the aggregate consideration at closing for the acquisition was approximately $7.6 million, subject to customary
post-closing adjustments. The consideration consisted of (i) approximately $1.6 million of cash, subject to certain adjustments, and
(ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing, the Company withheld 94,798 Indemnity
Holdback Shares, which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’
indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023. See Note 4 for more information regarding the acquisition of Scendia.
In
February 2023, the Company entered into a Controlled Equity Offering SM Sales Agreement (the “Sales Agreement”)
with Cantor Fitzgerald & Co., as sales agent (“Cantor”), pursuant to which the Company may offer and sell from time to
time, to or through Cantor, shares of the Company’s common stock having an aggregate offering price of up to $75,000,000.
Sales
of the shares, if any, pursuant to the Sales Agreement, may be made in sales deemed to be an “at the market offering” as
defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. Upon delivery of a placement notice and subject to
the terms and conditions of the Sales Agreement, Cantor agreed to use commercially reasonable efforts consistent with its normal trading
and sales practices, applicable state and federal law, rules and regulations and the rules of The Nasdaq Capital Market to sell the shares
from time to time based upon the Company’s instructions, including any price, time period or size limits specified by the Company.
The Company has no obligation to sell any of the shares under the Sales Agreement and may at any time suspend or terminate the offering
of its common stock pursuant to the Sales Agreement upon notice to Cantor and subject to other conditions. Cantor’s obligations
to sell the shares under the Sales Agreement are subject to satisfaction of certain conditions, including customary closing conditions.
Pursuant to the Sales Agreement, the Company will pay Cantor a commission of 3.0% of the aggregate gross proceeds from each sale of the
shares.
During
the three months ended September 30, 2023, the Company did not sell any shares of common stock pursuant to the Sales Agreement. During
the nine months ended September 30, 2023, the Company sold an aggregate of 26,143 shares of common stock for gross proceeds of approximately
$1,066,000 and net proceeds of approximately $1,034,000 pursuant to the Sales Agreement.
On
August 1, 2023, the Company closed the Applied Asset Purchase. The Applied Purchased Assets were purchased for an initial aggregate
purchase price of $15.25
million, consisting of (i) the Cash Closing Consideration, (ii) the Stock Closing Consideration and (iii) the Installment
Payments.
Restricted
Stock Awards
During
the nine months ended September 30, 2023, the Company issued restricted stock awards under the LTIP Plan which are subject to certain
vesting provisions and other terms and conditions set forth in each recipient’s respective restricted stock agreement. The Company
granted and issued 107,797 shares, net of forfeitures, of restricted common stock to employees, directors, and certain advisors of the
Company under the LTIP Plan during the nine months ended September 30, 2023. The fair value of these awards was $4,287,777 based on the
closing price of the Company’s common stock on the respective grant dates, which will be recognized as compensation expense on
a straight-line basis over the vesting period of the awards.
Share-based
compensation expense of $857,526 and $683,202 was recognized in “Selling, general and administrative expenses” in the accompanying
Consolidated Statements of Operations during the three months ended September 30, 2023 and 2022, respectively, and $2,582,163 and $1,971,537
was recognized during the nine months ended September 30, 2023 and 2022, respectively.
At
September 30, 2023, there was $3,980,624 of total unrecognized share-based compensation expense related to unvested share-based equity
awards. Unrecognized share-based compensation expense is expected to be recognized over a weighted-average period of 1.0 years.
Below
is a summary of restricted stock activity for the nine months ended September 30, 2023:
SUMMARY
OF RESTRICTED STOCK ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
Shares | | |
Weighted Average Grant Date Fair Value | |
Nonvested at beginning of period | |
| 181,102 | | |
$ | 22.89 | |
Granted | |
| 118,912 | | |
| 39.14 | |
Vested | |
| (129,342 | ) | |
| 22.84 | |
Forfeited | |
| (11,115 | ) | |
| 32.96 | |
Nonvested at September 30, 2023 | |
| 159,557 | | |
$ | 34.27 | |
Stock
Options
A
summary of the status of outstanding stock options at September 30, 2023 and changes during the nine months then ended is presented below:
SCHEDULE OF STOCK OPTION ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Options | | |
Price | | |
Contract
Life | |
Outstanding at beginning of period | |
| 146,191 | | |
$ | 10.65 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| (50,318 | ) | |
| 11.58 | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
Warrants
A
summary of the status of outstanding warrants to purchase common stock at September 30, 2023 and changes during the nine months then
ended is presented below:
SCHEDULE OF WARRANTS TO PURCHASE COMMON STOCK
| |
For the Nine Months Ended
September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Warrants | | |
Price | | |
Contract Life | |
Outstanding at beginning of period | |
| 16,725 | | |
$ | 10.80 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| - | | |
| - | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
NOTE
12 – INCOME TAXES
As
discussed in Notes 3 and 4, the Company recognized net deferred tax liabilities associated with the Precision Healing merger and the
Scendia acquisition. Prior to consideration of these deferred tax liabilities, the Company had net deferred tax assets in excess of the
deferred tax liabilities being recognized, however, a 100% valuation allowance had previously been provided against the Company’s
net deferred tax assets. As a result of the recording of the net deferred tax liabilities related to the Precision Healing merger and
the Scendia acquisition, the Company reviewed the valuation allowance and determined that it should be reduced by the amount of the deferred
tax liabilities that were recognized. This resulted in an income tax benefit of $1,702,890 and $5,844,796 in the three and nine months
ended September 30, 2022, respectively.
NOTE
13 – RELATED PARTIES
CellerateRX
Surgical Sublicense Agreement
The
Company has an exclusive, world-wide sublicense to distribute CellerateRX Surgical and HYCOL products into the surgical and wound care
markets from an affiliate of The Catalyst Group, Inc. (“Catalyst”), CGI Cellerate RX, which, prior to the Applied Asset Purchase,
licensed the rights to CellerateRX Surgical and HYCOL from Applied. Sales of CellerateRX Surgical comprised the substantial majority
of the Company’s sales during the nine months ended September 30, 2023 and 2022. In January 2021, the Company amended the term
of the Sublicense Agreement to extend the term to May 17, 2050, with automatic successive one-year renewals so long as annual net sales
of the licensed products exceed $1,000,000. The Company pays royalties based on the annual Net Sales of licensed products (as defined
in the Sublicense Agreement) consisting of 3% of all collected Net Sales each year up to $12,000,000, 4% of all collected Net Sales each
year that exceed $12,000,000 up to $20,000,000, and 5% of all collected Net Sales each year that exceed $20,000,000.
As
discussed further in Note 5, on August 1, 2023, the Company purchased certain assets from Applied, including the underlying
intellectual property of, as well as the rights to manufacture and sell, CellerateRX Surgical and HYCOL products. In connection with
the Applied Asset Purchase, Applied assigned its license agreement with CGI Cellerate RX to SMAT. Since the Closing, Sanara
indirectly makes intercompany royalty payments to SMAT at the same rate as set forth in the Sublicense Agreement. Ronald T. Nixon,
the Company’s Executive Chairman, is the founder and managing partner of Catalyst.
Product
License Agreements
In
July 2019, the Company executed a license agreement with Rochal, a related party, whereby the Company acquired an exclusive world-wide
license to market, sell and further develop antimicrobial products for the prevention and treatment of microbes on the human body utilizing
certain Rochal patents and pending patent applications. Currently, the products covered by the BIAKŌS License Agreement are BIAKŌS
Antimicrobial Wound Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser. Both products are 510(k) cleared. Mr. Nixon is a director
of Rochal, and indirectly a significant shareholder of Rochal, and through the potential exercise of warrants, a majority shareholder
of Rochal. Another one of the Company’s directors is also a significant shareholder and the current Chair of the board of directors
of Rochal.
In
October 2019, the Company executed the ABF License Agreement with Rochal whereby the Company acquired an exclusive world-wide license
to market, sell and further develop certain antimicrobial barrier film and skin protectant products for use in the human health care
market utilizing certain Rochal patents and pending patent applications. Currently, the products covered by the ABF License Agreement
are CuraShield Antimicrobial Barrier Film and a no sting skin protectant product.
In
May 2020, the Company executed a product license agreement with Rochal, whereby the Company acquired an exclusive world-wide license
to market, sell and further develop a debrider for human medical use to enhance skin condition or treat or relieve skin disorders, excluding
uses primarily for beauty, cosmetic, or toiletry purposes.
See
Note 10 for more information on these product license agreements.
Consulting
Agreement
Concurrent
with the Rochal asset purchase, in July 2021, the Company entered into a consulting agreement with Ann Beal Salamone pursuant to which
Ms. Salamone agreed to provide the Company with consulting services with respect to, among other things, writing new patents, conducting
patent intelligence, and participating in certain grant and contract reporting. In consideration for the consulting services to be provided
to the Company, Ms. Salamone is entitled to receive an annual consulting fee of $177,697, with payments to be paid once per month. The
consulting agreement has an initial term of three years, unless earlier terminated by the Company, and is subject to renewal. Ms. Salamone
is a director of the Company and is a significant shareholder and the current Chair of the board of directors of Rochal.
Catalyst
Transaction Advisory Services Agreement
In
March 2023, the Company entered into a Transaction Advisory Services Agreement (the “Catalyst Services Agreement”) effective
March 1, 2023 with Catalyst, a related party. Pursuant to the Catalyst Services Agreement, Catalyst, by and through its directors, officers,
employees and affiliates that are not simultaneously serving as directors, officers or employees of the Company (collectively, the “Covered
Persons”), agreed to perform certain transaction advisory, business and organizational strategy, finance, marketing, operational
and strategic planning, relationship access and corporate development services for the Company in connection with any merger, acquisition,
recapitalization, divestiture, financing, refinancing, or other similar transaction in which the Company may be, or may consider becoming,
involved, and any such additional services as mutually agreed upon in writing by and between Catalyst and the Company (the “Catalyst
Services”).
Pursuant
to the Catalyst Services Agreement, the Company agreed to reimburse Catalyst for (i) compensation actually paid by Catalyst to any of
the Covered Persons at a rate no more than a rate consistent with industry practice for the performance of services similar to the Catalyst
Services, as documented in reasonably sufficient detail, and (ii) all reasonable out-of-pocket costs and expenses payable to unaffiliated
third parties, as documented in customary expense reports, as each of (i) and (ii) is incurred in connection with the Catalyst Services
rendered under the Catalyst Services Agreement, with all reimbursements being contingent upon the prior approval of the Audit Committee
of the Company’s Board of Directors. The Company incurred $44,032
and $117,018
of costs pursuant to the Catalyst Services
Agreement in the three and nine months ended September 30, 2023, respectively.
ITEM
2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
The
following discussion and analysis of the financial condition and results of operations of Sanara MedTech Inc. (together with its wholly
owned or majority-owned subsidiaries on a consolidated basis, the “Company,” “Sanara MedTech,” “Sanara,”
“our,” “us,” or “we”) should be read in conjunction with the “Management’s Discussion
and Analysis of Financial Condition and Results of Operations” section and audited consolidated financial statements and related
notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 2022 and with the unaudited consolidated financial
statements and related notes thereto presented in this Quarterly Report on Form 10-Q.
CAUTIONARY
STATEMENT REGARDING FORWARD-LOOKING STATEMENTS
This
Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of the federal securities laws. Forward-looking
statements generally relate to future events or our future financial or operating performance. In some cases, you can identify forward-looking
statements because they contain words such as “aims,” “anticipates,” “believes,” “contemplates,”
“continue,” “could,” “estimates,” “expects,” “forecast,” “guidance,”
“intends,” “may,” “plans,” “possible,” “potential,” “predicts,”
“preliminary,” “projects,” “seeks,” “should,” “target,” “will”
or “would” or the negative of these words, variations of these words or other similar terms or expressions that concern our
expectations, strategy, plans, or intentions. Such forward-looking statements are subject to certain risks, uncertainties and assumptions
relating to factors that could cause actual results to differ materially from those anticipated in such statements, including, without
limitation, the following:
● | shortfalls
in forecasted revenue growth; |
● | our
ability to implement our comprehensive wound and skincare strategy through acquisitions and
investments and our ability to realize the anticipated benefits of such acquisitions and
investments; |
● | our
ability to meet our future capital requirements; |
● | our
ability to retain and recruit key personnel; |
● | the
intense competition in the markets in which we operate and our ability to compete within
our markets; |
● | the
failure of our products to obtain market acceptance; |
● | the
effect of security breaches and other disruptions; |
● | our
ability to maintain effective internal controls over financial reporting; |
● | our
ability to develop and commercialize new products and products under development, including
the manufacturing, distribution, marketing and sale of such products; |
● | our
ability to maintain and further grow clinical acceptance and adoption of our products; |
● | the
impact of competitors inventing products that are superior to ours; |
● | disruptions
of, or changes in, our distribution model, consumer base or the supply of our products; |
● | our
ability to manage product inventory in an effective and efficient manner; |
● | the
failure of third-party assessments to demonstrate desired outcomes in proposed endpoints; |
● | our
ability to successfully expand into wound and skincare virtual consult and other services; |
● | our
ability and the ability of our research and development partners to protect the proprietary
rights to technologies used in certain of our products and the impact of any claim that we
have infringed on intellectual property rights of others; |
● | our
dependence on technologies and products that we license from third parties; |
● | the
effects of current and future laws, rules, regulations and reimbursement policies relating
to the labeling, marketing and sale of our products and our planned expansion into wound
and skincare virtual consult and other services and our ability to comply with the various
laws, rules and regulations applicable to our business; and |
● | the
effect of defects, failures or quality issues associated with our products. |
For
a more detailed discussion of these and other factors that may affect our business and that could cause the actual results to differ
materially from those anticipated in forward-looking statements, see “Risk Factors” in Part I, Item 1A of our Annual Report
on Form 10-K for the year ended December 31, 2022, Part II, Item 1A “Risk Factors” and elsewhere in this Quarterly Report
on Form 10-Q. Forward-looking statements speak only as of the date on which they are made, and the Company does not assume any obligation
to update these forward-looking statements, except to the extent required by applicable securities laws.
OVERVIEW
We
are a medical technology company focused on developing and commercializing transformative technologies to improve clinical outcomes and
reduce healthcare expenditures in the surgical, chronic wound and skincare markets. Each of our products, services and technologies contributes
to our overall goal of achieving better clinical outcomes at a lower overall cost for patients regardless of where they receive care.
We strive to be one of the most innovative and comprehensive providers of effective surgical, wound and skincare solutions and are continually
seeking to expand our offerings for patients requiring treatments across the entire continuum of care in the United States.
We currently market several products across surgical
and chronic wound care applications and have multiple products in our pipeline. On August 1, 2023, we acquired, among other things, the
underlying intellectual property of, as well as the rights to manufacture and sell, CellerateRX Surgical Activated Collagen (Powder and
Gel) (“CellerateRX Surgical”), our primary product, and HYCOL Hydrolyzed Collagen (Powder and Gel) (“HYCOL”) from
Applied Nutritionals, LLC (“Applied”) for human wound care use (for more information regarding this acquisition, see the “Recent
Acquisitions” section below). Prior to such time, we had licensed the rights to these products through a sublicense agreement (the
“Sublicense Agreement”) with CGI Cellerate RX, LLC (“CGI Cellerate RX”), an affiliate of The Catalyst Group, Inc.
(“Catalyst”), both of which are related parties (for additional information regarding related parties, see the section titled
“Material Transactions with Related Parties” below). In connection with the asset purchase, Applied assigned its license agreement
with CGI Cellerate RX to a wholly owned subsidiary of the Company. We also license certain of our products from Rochal Industries, LLC
(“Rochal”) and Cook Biotech Inc.
In
July 2021, we acquired certain assets from Rochal, including, among others, intellectual property, four U.S. Food and Drug Administration
(“FDA”) 510(k) clearances, rights to license certain products and technologies currently under development, equipment and
supplies. As a result of the asset purchase, our pipeline now contains product candidates for mitigation of opportunistic pathogens and
biofilm, wound re-epithelialization and closure, necrotic tissue debridement and cell compatible substrates. Since our acquisition of
assets from Rochal, we have been developing additional products in our own product pipeline.
In
April 2022, we entered into a merger agreement through which Precision Healing Inc. (“Precision Healing”) became a wholly
owned subsidiary of the Company. Precision Healing is developing a diagnostic imager and lateral flow assay (“LFA”) for assessing
a patient’s wound and skin conditions. This comprehensive wound and skin assessment technology is designed to quantify biochemical
markers to determine the trajectory of a wound’s condition to enable better diagnosis and treatment protocol. During the first
quarter of 2023, we submitted a 510(k) premarket notification to the FDA for the Precision Healing diagnostic imager. We are evaluating when or if we will submit a 510(k) premarket notification for the Precision Healing LFA.
In
July 2022, we entered into a membership interest purchase agreement with Scendia Biologics, LLC (“Scendia”) and Ryan Phillips
(“Phillips”) pursuant to which we acquired 100% of the issued and outstanding membership interests in Scendia from Phillips.
Since our acquisition of Scendia, we have been selling a full line of regenerative and orthobiologic technologies including (i) TEXAGEN
Amniotic Membrane Allograft (“TEXAGEN”), (ii) BiFORM Bioactive Moldable Matrix (“BiFORM”), (iii) ACTIGEN Verified
Inductive Bone Matrix (“ACTIGEN”) and (iv) ALLOCYTE Advanced Cellular Bone Matrix (“ALLOCYTE”).
In
November 2022, we established a partnership with InfuSystem Holdings, Inc. (“InfuSystem”) focused on delivering a complete
wound care solution targeted at improving patient outcomes, lowering the cost of care, and increasing patient and provider satisfaction.
The partnership is expected to enable InfuSystem to offer innovative products, including Cork Medical, LLC’s negative pressure
wound therapy devices and supplies, and our advanced wound care product line and associated services to new customers.
COMPREHENSIVE
VALUE-BASED CARE STRATEGY
In
June 2020, we formed a subsidiary, United Wound and Skin Solutions, LLC (“UWSS” or “WounDerm”), to hold certain
investments and operations in wound and skincare virtual consult services. Through WounDerm, we plan to offer a comprehensive wound and
skincare solution and partner with value-based care providers with the dual goal of lowering the cost to treat wounds while improving
clinical outcomes.
Our
comprehensive solution consists of four key components: diagnostics, virtual consult services for wound care and dermatology, proprietary
efficacious products, and a wound care and dermatology specific electronic medical record (“EMR”) and mobile application.
We expect these components will work synergistically to allow clinicians to analyze and treat wound and dermatology conditions more efficiently
than the current standard of care:
●
Diagnostics – Our proprietary imager and LFA currently under development, which we recently acquired through our acquisition
of Precision Healing, are designed to quantify key biomarkers that dictate the trajectory of wound healing and identify deficiencies
to aid in treatment. Ultimately, we believe that our diagnostics will lead to treatment algorithms based on the data collected by the
Precision Healing technology.
●
Virtual Consult Services – Through our exclusive affiliation with Direct Dermatology Inc., we can offer virtual consult
services for wound care and dermatology provided by experienced, specialized physicians and clinicians.
●
Proprietary Products – We currently offer products for improving patient outcomes by addressing conditions that impact wound
healing. We are currently conducting multiple studies to prove the efficacy of our products while developing and exploring new products
and opportunities in our six focus areas of (1) debridement, (2) biofilm removal, (3) hydrolyzed collagen, (4) advanced biologics, (5)
negative pressure wound therapy products and (6) the oxygen delivery system segment of the wound and skincare market.
●
EMR and Mobile Application – Our EMR and mobile application were developed specifically for wound care and dermatology.
We are currently developing the capability for the EMR and mobile application to offer wound tracking analytics, recommended treatments
and decision support and automated referrals.
We
believe that by offering a proprietary comprehensive solution for wound care and dermatology, we will be a value-added partner for providers
in value-based care programs, such as Medicare Advantage and other risk-based contracts.
RECENT
ACQUISITIONS
Precision
Healing
In
April 2022, we closed a merger transaction with Precision Healing, pursuant to which Precision Healing became a wholly owned subsidiary
of the Company. Precision Healing is developing a diagnostic imager and LFA for assessing a patient’s wound and skin conditions.
This comprehensive wound and skin assessment technology is designed to quantify biochemical markers to determine the trajectory of a
wound’s condition to enable better diagnosis and treatment protocol.
Pursuant
to the merger agreement, among other things, we agreed to (i) pay the holders of Precision Healing common stock and preferred stock closing
consideration consisting of 165,738 shares of our common stock, which was issued to accredited investors, and $125,966 in cash, which
was paid to stockholders who were not accredited investors, (ii) pay approximately $0.6 million of transaction expenses on behalf of
the equity holders of Precision Healing, (iii) assume all outstanding options and warrants of Precision Healing and (iv) pay, subject
to the achievement of certain performance thresholds, earnout consideration of up to $10.0 million which is payable in cash or, at our
election, is payable to accredited investors in shares of our common stock.
Scendia
In
July 2022, we entered into a membership interest purchase agreement by and among the Company, Scendia and Phillips pursuant to which
we acquired 100% of the issued and outstanding membership interests in Scendia from Phillips. Scendia provides clinicians and surgeons
with a full line of regenerative and orthobiologic technologies. Beginning in early 2022, the Company began co-promoting certain products
with Scendia, including: (i) TEXAGEN, (ii) BiFORM, (iii) ACTIGEN and (iv) ALLOCYTE. Prior to the acquisition, Scendia owned 50% of the
issued and outstanding membership interests in Sanara Biologics, LLC (“Sanara Biologics”) and the Company owned the remaining
50% of the membership interests. As a result of the acquisition, the Company indirectly acquired all the interests in Sanara Biologics,
such that the Company now holds 100% of the issued and outstanding equity interests in Sanara Biologics.
Pursuant
to the purchase agreement, the aggregate consideration at closing for the acquisition was $7.6 million, which consisted of (i) a $1.6
million cash payment, subject to certain adjustments, and (ii) 291,686 shares of our common stock, with an agreed upon value of $6.0
million. Pursuant to the purchase agreement, at closing, we withheld 94,798 shares of common stock with an agreed upon value of $1.95
million (the “Indemnity Holdback Shares”), which such Indemnity Holdback Shares were withheld to the extent provided in the
purchase agreement to satisfy Phillips’ indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash and stock consideration, the purchase agreement provides that Phillips is entitled to receive two potential earnout
payments, payable on an annual basis, not to exceed $10.0 million in the aggregate. The earnout consideration is payable to Phillips
in cash or, at our election, in up to 486,145 shares of our common stock upon the achievement of certain performance thresholds relating
to net revenue attributable to sales of Scendia products during the two-year period following the closing. We made the first earnout
payment of approximately $693,000 in cash in August 2023. We expect the second earnout payment to be made in the third quarter of 2024.
Applied
Asset Purchase
On
August 1, 2023, we entered into an Asset Purchase Agreement (the “Applied Purchase Agreement”) by and among the Company,
as guarantor, Sanara MedTech Applied Technologies, LLC, a wholly owned subsidiary of the Company (“SMAT”), Applied, The
Hymed Group Corporation (“Hymed” and together with Applied, the “Sellers”), and Dr. George D. Petito (the
“Owner”), pursuant to which SMAT acquired certain assets of the Sellers and the Owner, including, among others, the
Sellers’ and Owner’s inventory, intellectual property, manufacturing and related equipment, goodwill, rights and claims,
other than certain excluded assets, all as more specifically set forth in the Applied Purchase Agreement (collectively, the
“Applied Purchased Assets”), and assumed certain Assumed Liabilities (as defined in the Applied Purchase Agreement),
upon the terms and subject to the conditions set forth in the Applied Purchase Agreement (such transaction, the “Applied Asset
Purchase”). The Applied Purchased Assets include the underlying intellectual property of, as well as the rights to manufacture
and sell, CellerateRX Surgical and HYCOL products for human wound care use.
The
Applied Purchased Assets were purchased for an initial aggregate purchase price of $15.25 million, consisting of (i) $9.75 million in
cash (the “Cash Closing Consideration”), (ii) 73,809 shares of our common stock (the “Stock Closing Consideration”)
with an agreed upon value of $3.0 million and (iii) $2.5 million in cash (the “Installment Payments”), to be paid in four
equal installments on each of the next four anniversaries of the closing of the Applied Asset Purchase (the “Closing”).
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive up to an additional $10.0 million (the “Applied Earnout”), which is payable to the
Sellers in cash, upon the achievement of certain performance thresholds relating to SMAT’s collections from net sales of a collagen-based
product currently under development. Upon expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned
the entirety of the Applied Earnout, SMAT shall pay the Sellers a pro-rata amount of the Applied Earnout based on collections from net
sales of the product, with such amount to be due credited against any Applied Earnout payments already made by SMAT (the “True-Up
Payment”). The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already made by SMAT, may be earned
at any point in the future, including after the True-Up Payment is made.
RECENT
DEVELOPMENTS
Professional
Services Agreement
In
connection with the Applied Asset Purchase and pursuant to the Applied Purchase Agreement, effective August 1, 2023, we entered into
a professional services agreement (the “Petito Services Agreement”) with the Owner, pursuant to which the Owner, as an independent
contractor, agreed to provide certain services to us, including, among other things, assisting with the development of products already
in development and assisting with research, development, formulation, invention and manufacturing of any future products (the “Petito
Services”). As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of $12,000 per month
during the term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual collections from net
sales of certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment equal to five percent
(5%) for the first $50.0 million in aggregate collections from net sales of certain future products and a royalty payment of two and
one-half percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding $50.0 million but
up to $100.0 million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted by the Company
and (v) $1.0 million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect to the incentive
payments described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
The
Petito Services Agreement has an initial term of three years and is subject to automatic successive one-month renewals unless earlier
terminated in accordance with its terms. The Petito Services Agreement may be terminated upon the Owner’s death or disability or
by us or the Owner “For Cause” (as defined in the Petito Services Agreement); provided, however, that the base salary described
in (i) of the foregoing paragraph shall survive termination through the three-year initial term and the royalty payments and incentive
payments described in (ii)-(v) of the foregoing paragraph shall survive termination of the Petito Services Agreement.
Loan
Agreement
In
connection with the entry into the Applied Purchase Agreement, on August 1, 2023, we, as guarantor, and SMAT, as borrower, entered into
a loan agreement (the “Loan Agreement”) with Cadence Bank (the “Bank”) providing for, among other things, an
advancing term loan in the aggregate principal amount of $12.0 million (the “Term Loan”). Pursuant to the Loan Agreement,
the Bank agreed to make, at any time and from time to time prior to February 1, 2024, one or more advances to SMAT. On August 1, 2023,
the Bank made an advance under the Term Loan for $9.75 million, the proceeds of which were used to fund the Cash Closing Consideration
for the Applied Asset Purchase. For more information regarding the Loan Agreement, see the “Liquidity and Capital Resources”
section below.
COMPONENTS
OF RESULTS OF OPERATIONS
Sources
of Revenues
Our
revenue is derived primarily from sales of our soft tissue repair and bone fusion products to hospitals and other acute care facilities.
In particular, the substantial majority of our product sales revenue is derived from sales of CellerateRX surgical powder. Our revenue
is driven by direct orders shipped by us to our customers, and to a lesser extent, direct sales to customers through delivery at the
time of procedure by one of our sales representatives. We generally recognize revenue when a purchase order is received from the customer
and our product is received by the customer.
Revenue
streams from product sales and royalties are summarized below for the three and nine months ended September 30, 2023 and 2022.
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Soft tissue repair products | |
$ | 13,634,316 | | |
$ | 10,969,271 | | |
$ | 39,756,539 | | |
$ | 28,296,919 | |
Bone fusion products | |
| 2,340,382 | | |
| 2,025,050 | | |
| 7,392,740 | | |
| 2,078,903 | |
Royalty revenue | |
| 50,250 | | |
| 50,250 | | |
| 150,750 | | |
| 150,750 | |
Total Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
We
recognize royalty revenue from a development and licensing agreement with BioStructures, LLC. We record revenue each calendar quarter
as earned per the terms of the agreement which stipulates that we will receive quarterly royalty payments of at least $50,250. Under
the terms of the development and license agreement, royalties of 2.0% are recognized on sales of products containing our patented resorbable
bone hemostasis. The minimum annual royalty due to us is $201,000 per year through the end of 2023. These royalties are payable in quarterly
installments of $50,250. To date, royalties related to this development and licensing agreement have not exceeded the annual minimum
of $201,000 ($50,250 per quarter).
Cost
of Goods Sold
Cost
of goods sold consists primarily of the acquisition costs from the manufacturers of our licensed products, raw material costs for certain
components sourced directly by us and all related royalties due as a result of the sale of our products. Our gross profit represents
total net revenue less the cost of goods sold, and gross margin represents gross profit expressed as a percentage of total revenue.
Operating
Expenses
Selling,
general and administrative (“SG&A”) expenses consist primarily of salaries, sales commissions, benefits, bonuses and
stock-based compensation. SG&A also includes outside legal counsel fees, audit fees, insurance premiums, rent and other corporate
expenses. We expense all SG&A expenses as incurred.
Research
and development (“R&D”) expenses include costs related to enhancements to our currently available products and additional
investments in our product, services and technologies development pipeline. This includes personnel-related expenses, including salaries
and benefits for all personnel directly engaged in R&D activities, contracted services, materials, prototype expenses and allocated
overhead, which is comprised of lease expense and other facilities-related costs. We expense R&D costs as incurred. We generally
expect that R&D expenses will increase as we continue to support product enhancements and bring new products to market.
Depreciation
and amortization expenses include depreciation of fixed assets and amortization of intangible assets that have a finite life, such as
product licenses, patents and intellectual property, customer relationships and assembled workforces.
Change
in fair value of earnout liabilities represents our measurement of the change in fair value at the balance sheet date of our earnout
liabilities that were established at the time of our Precision Healing, Scendia and Applied acquisitions.
Other
Expense
Other
expense is primarily comprised of losses on equity method investments, interest expense, accretion expense and other nonoperating activities.
RESULTS
OF OPERATIONS
Net
Revenue. For the three months ended September 30, 2023, we generated net revenue of $16.0 million compared to net revenue
of $13.0 million for the three months ended September 30, 2022, a 23% increase from the prior year period. For the nine months ended
September 30, 2023, we generated net revenue of $47.3 million compared to net revenue of $30.5 million for the nine months ended September
30, 2022, a 55% increase from the prior year period. The higher net revenue for the three and nine months ended September 30, 2023 were
primarily due to increased sales of soft tissue repair products and, to a lesser extent, bone fusion products, as a result of our increased
market penetration and geographic expansion, additional revenues as a result of the Scendia acquisition and our continuing strategy to
expand our independent distribution network in both new and existing U.S. markets.
During
the third quarter of 2022, we began to experience supply issues with the ALLOCYTE product line. During the fourth quarter of 2022 and the nine months
ended September 30, 2023, we were unable to fill certain orders for this product, which negatively impacted our sales growth. The supply constraint was caused by significant supplier limits on qualifying
eligible donor tissue and supplier necessity to subcontract all processing to secondary suppliers. We have
since expanded the ALLOCYTE product line with the release of ALLOCYTE Plus Advanced Viable Bone Matrix (“ALLOCYTE Plus”),
which is processed by an alternative supplier with in-house processing capabilities. Our first sales of ALLOCYTE Plus occurred in October
2023. We have a sufficient supply of ALLOCYTE Plus to meet currently expected demand and believe we have measures in place to regularly
stock the product in the future.
Cost
of goods sold. Cost of goods sold for the three months ended September 30, 2023, was $1.8 million, compared to costs of goods
sold of $2.2 million for the three months ended September 30, 2022. Cost of goods sold for the nine months ended September 30, 2023,
was $6.1 million, compared to costs of goods sold of $4.0 million for the nine months ended September 30, 2022. The decrease in cost
of goods sold for the three months ended September 30, 2023 was primarily due to the elimination of royalty expense on CellerateRX on
a consolidated basis as a result of the Applied Asset Purchase. The increase in cost of goods sold for the nine months ended September
30, 2023 was primarily due to higher sales volume as a result of organic sales growth and our acquisition of Scendia. Gross margins were
approximately 87% for both nine-month periods ended September 30, 2023 and 2022. The gross margins for the nine months ended September
30, 2023 included lower margins realized on sales of certain Scendia products offset by higher margins realized due to the elimination
in consolidation of the CellerateRX royalty expense under the Sublicense Agreement.
Selling,
general and administrative expenses. SG&A expenses for the three months ended September 30, 2023, were $13.9 million compared
to SG&A expenses of $12.1 million for the three months ended September 30, 2022. SG&A expenses for the nine months ended September
30, 2023, were $40.7 million compared to SG&A expenses of $31.9 million for the nine months ended September 30, 2022. The higher
SG&A expenses for the three and nine months ended September 30, 2023 were primarily due to higher direct sales and marketing expenses,
which accounted for approximately $1.0 million and $6.8 million, respectively, or 56% and 77%, respectively, of the increases compared
to the prior year periods. The higher direct sales and marketing expenses for the three and nine months ended September 30, 2023 were
primarily attributable to an increase in sales commissions of $0.7 million and $5.9 million, respectively, as a result of higher product
sales. The nine months ended September 30, 2023 also included $0.8 million of increased costs as a result of sales force expansion and
operational support. We expect our SG&A expenses to decline as a percentage of net revenues as our sales growth outpaces the costs
of sales force expansion and corporate overhead.
Research
and development expenses. R&D expenses for the three months ended September 30, 2023, were $1.0 million compared to $1.1
million for the three months ended September 30, 2022. R&D expenses for the nine months ended September 30, 2023, were $3.5 million
compared to $2.3 million for the nine months ended September 30, 2022. The higher R&D expenses for the nine months ended September
30, 2023 were primarily due to costs related to the Precision Healing diagnostic imager and LFA. R&D expenses for the three and nine
months ended September 30, 2023 also included costs associated with ongoing development projects for our currently licensed products.
Depreciation
and amortization expense. Depreciation and amortization expense for the three months ended September 30, 2023, was $1.0 million
compared to $0.8 million for the three months ended September 30, 2022. The higher depreciation and amortization expense during the three
months ended September 30, 2023 was primarily due to the amortization of intangible assets acquired as part of the Applied Asset Purchase.
Depreciation and amortization expense for the nine months ended September 30, 2023, was $2.6 million compared to $1.6 million for the
nine months ended September 30, 2022. The higher depreciation and amortization expense during the nine months ended September 30, 2023
was primarily due to the amortization of intangible assets acquired as part of the Precision Healing, Scendia and Applied transactions.
Change
in fair value of earnout liabilities. Change in fair value of earnout liabilities was a benefit of $0.7 million for the three
months ended September 30, 2023 compared to expense of $0.1 million for the three months ended September 30, 2022. Change in fair value
of earnout liabilities was a benefit of $1.5 million for the nine months ended September 30, 2023 compared to an expense of $0.2 million
for the nine months ended September 30, 2022. The current year benefits are as a result of a decrease in the estimated fair value of
the earnout liabilities established at the time of our Precision Healing and Scendia acquisitions. The decrease in the estimated fair
value was due to a change in the discount factor utilized in the valuation models, a decrease in the projected undiscounted amounts to
be paid, as well as adjustments to the projected timing of the payments to be made, partially offset by accretion. The prior year period
expenses were due to the accretion of the earnout liabilities.
Other
expense. Other expense for the three months ended September 30, 2023 was $0.2 million compared to zero for the three months ended
September 30, 2022. Other expense for the nine months ended September 30, 2023 was $0.2 million compared to $0.4 million for the nine months
ended September 30, 2022. Other expense for the three and nine months ended September 30, 2023 included interest expense, accretion expense and amortization
of debt issuance costs related to the Term Loan entered into in conjunction with the Applied Asset Purchase. Other expense for the nine
months ended September 30, 2022 included losses from our equity method investment in Precision Healing prior to our acquisition of the
remaining interests in April 2022.
Loss
before income taxes. We had a loss before income taxes of $1.1 million for the three months ended September 30, 2023, compared
to a loss before income taxes of $3.2 million for the three months ended September 30, 2022. For the nine months ended September 30,
2023, we had a loss before income taxes of $4.2 million, compared to a loss before income taxes of $9.8 million for the nine months ended
September 30, 2022. The lower loss for the three and nine months ended September 30, 2023 was due to operating expenses increasing at
a slower rate than net sales in addition to the benefit recorded as a result of the change in fair value of earnout liabilities.
Income
tax benefit. As discussed in Note 12 to the accompanying unaudited consolidated financial statements, we recognized net deferred
tax liabilities associated with the Precision Healing merger and the Scendia acquisition. Prior to consideration of these deferred tax
liabilities, we had net deferred tax assets in excess of the deferred tax liabilities being recognized, however, a 100% valuation allowance
had previously been provided against our net deferred tax assets. As a result of the recording of the net deferred tax liabilities related
to the Precision Healing merger and the Scendia acquisition, we reviewed the valuation allowance and determined that it should be reduced
by the amount of the deferred tax liabilities that were recognized. This resulted in recognition of an income tax benefit of $1.7 million
and $5.8 million in the three and nine months ended September 30, 2022, respectively.
Net
loss. For the three months ended September 30, 2023, we had a net loss of $1.1 million, compared to a net loss of $1.5 million
for the three months ended September 30, 2022. For the nine months ended September 30, 2023, we had a net loss of $4.2 million, compared
to a net loss of $3.9 million for the nine months ended September 30, 2022.
LIQUIDITY
AND CAPITAL RESOURCES
Cash
on hand at September 30, 2023 was $6.2 million, compared to $9.0 million at December 31, 2022. Historically, we have financed our operations
primarily from the sale of equity securities. In February 2023, we entered into a Controlled Equity Offering SM Sales Agreement
(the “Sales Agreement”) with Cantor Fitzgerald & Co., as sales agent (“Cantor”), pursuant to which we may
offer and sell from time to time, to or through Cantor, shares of our common stock having an aggregate offering price of up to $75.0
million.
Sales
of the shares, if any, pursuant to the Sales Agreement, may be made in sales deemed to be an “at the market offering” as
defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. Upon delivery of a placement notice and subject to
the terms and conditions of the Sales Agreement, Cantor agreed to use commercially reasonable efforts consistent with its normal trading
and sales practices, applicable state and federal law, rules and regulations and the rules of The Nasdaq Capital Market to sell the shares
from time to time based upon our instructions, including any price, time period or size limits specified by us. We have no obligation
to sell any of the shares under the Sales Agreement and may at any time suspend or terminate the offering of our common stock pursuant
to the Sales Agreement upon notice to Cantor and subject to other conditions. Cantor’s obligations to sell the shares under the
Sales Agreement are subject to satisfaction of certain conditions, including customary closing conditions. Pursuant to the Sales Agreement,
we will pay Cantor a commission of 3.0% of the aggregate gross proceeds from each sale of the shares.
During
the three months ended September 30, 2023, we did not sell any shares of common stock pursuant to the Sales Agreement. During the nine
months ended September 30, 2023, we sold an aggregate of 26,143 shares of common stock for gross proceeds of approximately $1.1 million
and net proceeds of approximately $1.0 million pursuant to the Sales Agreement.
We
expect our future needs for cash to include funding potential acquisitions, further developing our products, services and technologies
pipeline and clinical studies, expanding our sales force, repayment of debt as it becomes due and for general corporate purposes. Based
on our current plan of operations, we believe our cash on hand, when combined with expected cash flows from operations and proceeds from
the Term Loan discussed above, will be sufficient to fund our growth strategy and to meet our anticipated operating expenses and capital
expenditures for at least the next twelve months.
Precision
Healing Merger
In
November 2020, we entered into agreements to purchase shares of Series A Convertible Preferred Stock (the “Series A Stock”)
of Precision Healing for an aggregate purchase price of $600,000. In 2021, we made additional purchases of Series A Stock: $600,000 in
February, $500,000 in June, $500,000 in October, and $600,000 in December.
In
April 2022, we closed a merger transaction with Precision Healing pursuant to which Precision Healing became our wholly owned subsidiary.
Pursuant to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock, other than the Company,
were entitled to receive closing consideration, consisting of $125,966 in cash, which was paid to stockholders who were not accredited
investors, 165,738 shares of our common stock, which was paid only to accredited investors, and the payment in cash of approximately
$0.6 million of transaction expenses of Precision Healing. We recorded the issuance of the 165,738 shares to accredited investors and
cash payments to nonaccredited investors based on the closing price per share of our common stock on April 4, 2022, which was $30.75.
Upon
the closing of the merger, the outstanding Precision Healing options previously granted under the Precision Healing Inc. 2020 Stock Option
and Grant Plan (the “Precision Healing Plan”) converted, pursuant to their terms, into options to acquire an aggregate of
144,191 shares of our common stock with a weighted average exercise price of $10.71 per share. These options expire between August 2030
and April 2031. In addition, outstanding and unexercised Precision Healing warrants converted into rights to receive warrants to purchase
(i) 4,424 shares of our common stock with an initial exercise price of $7.32 per share and an expiration date of April 22, 2031, and
(ii) 12,301 shares of our common stock with an initial exercise price of $12.05 per share and an expiration date of August 10, 2030.
Concurrent with the assumption of the Precision Healing Plan, we terminated the ability to offer future awards under the Precision Healing
Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to Accounting Standards Codification Topic 805, Business Combinations. The earnout consideration is payable in cash or, at our
election, is payable to accredited investors in shares of our common stock at a price per share equal to the greater of (i) $27.13 or
(ii) the average closing price of our common stock for the 20 trading days prior to the date such earnout consideration is due and payable.
Pursuant to the merger agreement, a minimum percentage of the earnout consideration may be required to be issued to accredited investors
in shares of our common stock for tax purposes. The amount and composition of the portion of earnout consideration payable is subject
to adjustment and offsets as set forth in the merger agreement. We do not anticipate making an earnout consideration payment prior to
January 2025.
Scendia
Acquisition
In
July 2022, we entered into a membership interest purchase agreement by and among the Company, Scendia and Phillips pursuant to which,
and in accordance with the terms and conditions set forth therein, we acquired 100% of the issued and outstanding membership interests
in Scendia from Phillips.
Pursuant
to the purchase agreement, Phillips was entitled to receive closing consideration consisting of (i) approximately $1.6 million of cash,
subject to certain adjustments, and (ii) 291,686 shares of our common stock. Pursuant to the purchase agreement, at closing, we withheld
the Indemnity Holdback Shares, which Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy
Phillips’ indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate. The earnout consideration is
payable to Phillips in cash or, at our election, in up to 486,145 shares of our common stock upon the achievement of certain performance
thresholds relating to net revenue attributable to sales of Scendia products during the two-year period following the closing. We made
the first earnout payment of approximately $693,000 in cash in August 2023. We expect the second earnout payment to be made in the third
quarter of 2024.
Applied
Asset Purchase
On
August 1, 2023, we entered into the Applied Purchase Agreement by and among the Company, SMAT, Hymed, Applied and the Owner, pursuant
to which SMAT acquired the Applied Purchased Assets and assumed certain Assumed Liabilities upon the terms and subject to the conditions
set forth in the Applied Purchase Agreement. The transaction closed on August 1, 2023. The Applied Purchased Assets were purchased for
an initial aggregate purchase price of $15.25 million, consisting of (i) $9.75 million in cash, (ii) 73,809 shares of our common stock,
with an agreed upon value of $3.0 million and (iii) $2.5 million in cash, to be paid in four equal installments on each of the next four
anniversaries of the Closing.
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive up to an additional $10.0 million, which is payable to the Sellers in cash, upon the achievement
of certain performance thresholds relating to SMAT’s collections from net sales of a collagen-based product currently under development.
Upon expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned the entirety of the Applied Earnout,
SMAT shall pay the Sellers the True-Up Payment. The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already
made by SMAT, may be earned at any point in the future, including after the True-Up Payment is made.
Since
the closing of the Applied Asset Purchase, we make intercompany royalty payments to SMAT at the same rate as set forth in the Sublicense
Agreement. SMAT intends to use the royalties received to repay borrowings under the Term Loan. As described under “Loan Agreement”
below, SMAT is required to maintain compliance with certain maintenance covenants and is limited in its ability to distribute or lend
cash to the Company without consent of the Bank.
Loan
Agreement
In
connection with the entry into the Applied Purchase Agreement, on August 1, 2023, we, as guarantor, and SMAT, as borrower, entered into
the Loan Agreement with the Bank providing for, among other things, a Term Loan in the aggregate principal amount of $12.0 million, which
was evidenced by an advancing promissory note. Pursuant to the Loan Agreement, the Bank agreed to make, at any time and from time to
time prior to February 1, 2024, one or more advances to SMAT.
The
proceeds of the advances under the Loan Agreement will be used for working capital and for purposes of financing up to one hundred percent
(100%) of the Cash Closing Consideration and Installment Payments for the Applied Asset Purchase and related fees and expenses, including
any subsequent payments that may be due to the Sellers after the Closing. On August 1, 2023, the Bank, at the request of SMAT, made an
advance for $9.75 million. The proceeds from the advance were used to fund the Cash Closing Consideration for the Applied Asset Purchase.
Advances
under the Term Loan will begin amortizing in monthly installments commencing on August 5, 2024. All remaining unpaid balances under the
Term Loan are due and payable in full on August 1, 2028 (the “Maturity Date”). SMAT may prepay amounts due under the Term
Loan. All accrued but unpaid interest on the unpaid principal balance of outstanding advances is due and payable monthly, beginning on
September 5, 2023 and continuing monthly on the fifth day of each month thereafter until the Maturity Date. The unpaid principal balance
of outstanding advances bears interest, subject to certain conditions, at the lesser of the Maximum Rate (as defined in the Loan Agreement)
or the Base Rate, which is for any day, a rate per annum equal to the term secured overnight financing rate (Term SOFR) (as administered
by the Federal Reserve Bank of New York) for a one-month tenor in effect on such day plus three percent (3.0%).
The
obligations of SMAT under the Loan Agreement and the other loan documents delivered in connection therewith are guaranteed by us and
are secured by a first priority security interest in substantially all of the existing and future assets of SMAT.
The
Loan Agreement contains customary representations and warranties and certain covenants that limit (subject to certain exceptions) the
ability of SMAT and us to, among other things, (i) create, assume or guarantee certain liabilities, (ii) create, assume or suffer liens
securing indebtedness, (iii) make or permit loans and advances, (iv) acquire any assets outside the ordinary course of business, (v)
consolidate, merge or sell all or a material part of its assets, (vi) pay dividends or other distributions on, or redeem or repurchase,
interest in an obligor, including us as guarantor, (vii) cease, suspend or materially curtail business operations or (viii) engage in
certain affiliate transactions. In addition, the Loan Agreement contains financial covenants that require SMAT to maintain (i) a minimum
Debt Services Coverage Ratio and (ii) a maximum Cash Flow Leverage Ratio, in each case, as defined and calculated according to the procedures
set forth in the Loan Agreement. Pursuant to the Loan Agreement, in the event that SMAT fails to comply with the financial covenants
described above, we are required to contribute cash to SMAT in an amount equal to the amount required to satisfy the financial covenants.
SMAT is limited in its ability to distribute or lend cash to the Company without consent of the Bank.
Pursuant
to the Loan Agreement, starting with the three months ended September 30, 2023 and for each quarter thereafter, SMAT will be required
to maintain a minimum Debt Service Coverage Ratio (as defined below) of 1.2 to 1.0, which ratio is calculated as of the last day of the
applicable fiscal quarter. The “Debt Service Coverage Ratio” is the ratio of (a) the sum of the following during the preceding
twelve (12) month period, subject to annualization in certain circumstances: (i) earnings before interest, taxes, depreciation, amortization,
stock compensation expense and gains or losses on sales of assets outside the ordinary course of business (“EBITDA”) minus
(ii) capital expenditures, minus (iii) cash taxes, minus (iv) dividends and distributions, to (b) the sum of (i) the current portion
of long-term debt, (ii) Installment Payments made during the preceding twelve (12) month period and (iii) interest expense during the
preceding twelve (12) month period, subject to annualization in certain circumstances. As of September 30, 2023, following a cash
contribution from Sanara (as described below), SMAT’s Debt Service Coverage Ratio was 1.3 to 1.0.
The Loan Agreement also requires SMAT to, subject
to certain conditions, maintain a maximum Cash Flow Leverage Ratio (as defined below) of not more than (a) 4.5 to 1.0 as of the last day
of the fiscal quarter ending on September 30, 2023, (b) 4.0 to 1.0 as of the last day of each fiscal quarter ending on December 31, 2023,
and March 31, 2024, (c) 3.5 to 1.0 as of the last day of each fiscal quarter ending on June 30, 2024, and September 30, 2024, and (d)
3.0 to 1.0 as of the last day of each fiscal quarter thereafter. The “Cash Flow Leverage Ratio” is the ratio of all Funded
Debt (as defined in the Loan Agreement) to certain multiples of EBITDA during the preceding twelve (12) month period, subject to annualization
in certain circumstances. SMAT was in compliance with the financial covenants under the Loan Agreement as of September 30, 2023. Due to
the short period of time between the signing of the Loan Agreement and the end of the third quarter, we contributed an immaterial amount
of cash to SMAT in order to permit SMAT to be in compliance with the financial covenants under the Loan Agreement. As of September 30,
2023, following a cash contribution from Sanara, SMAT’s Cash Flow Leverage Ratio was 4.5 to 1.0.
The
Loan Agreement also contains customary events of default. If such an event of default occurs, the Bank would be entitled to take various
actions, including the acceleration of amounts due under the Loan Agreement and actions permitted to be taken by a secured creditor.
Cash
Flow Analysis
For
the nine months ended September 30, 2023, net cash used in operating activities was $2.4 million compared to $4.9 million used in operating
activities for the nine months ended September 30, 2022. The lower use of cash was due to net revenue growth outpacing the growth of
our cash operating expenses and timing of cash expenditures for certain accrued payables.
For
the nine months ended September 30, 2023, net cash used in investing activities was $10.2 million compared to $3.1 million used in investing
activities during the nine months ended September 30, 2022. The higher use of cash used in investing activities during the nine months
ended September 30, 2023 was primarily due to cash paid pursuant to the Applied Asset Purchase.
For
the nine months ended September 30, 2023, net cash provided by financing activities was $9.8 million as compared to $0.3 million used
in financing activities for the nine months ended September 30, 2022. The cash provided by financing activities during the nine months
ended September 30, 2023 was due to net loan proceeds of $9.7 million utilized for the Applied Asset Purchase and net proceeds received
pursuant to sales of our common stock of $1.0 million, partially offset by the Scendia earnout payment of $0.7 million and the net settlement
of equity-based awards, which totaled $0.2 million.
MATERIAL
TRANSACTIONS WITH RELATED PARTIES
CellerateRX
Surgical Sublicense Agreement
We
have an exclusive, world-wide sublicense to distribute CellerateRX Surgical and HYCOL products into the surgical and wound care
markets from an affiliate of Catalyst, CGI Cellerate RX, which, prior to the Applied Asset Purchase, licensed the rights to
CellerateRX from Applied. Sales of CellerateRX Surgical comprised the substantial majority of our sales during the nine months ended
September 30, 2023 and 2022. In January 2021, we amended the term of the Sublicense Agreement to extend the term to May 17, 2050,
with automatic successive one-year renewals so long as annual net sales of the licensed products exceed $1.0 million. We pay
royalties based on the annual Net Sales of licensed products (as defined in the Sublicense Agreement) consisting of 3% of all
collected Net Sales each year up to $12.0 million, 4% of all collected Net Sales each year that exceed $12.0 million up to $20.0
million, and 5% of all collected Net Sales each year that exceed $20.0 million. For the three months ended September 30, 2023 and
2022, royalty expense was a benefit of approximately $9,000 for the three months ended September 30, 2023 due to the reversal of an
accrual and $0.4 million of expense, respectively, under the terms of this agreement. For the nine months ended September 30, 2023
and 2022, royalty expense was $1.1 million and $1.2 million, respectively, under the terms of this agreement. Ronald T. Nixon, our
Executive Chairman, is the founder and managing partner of Catalyst.
As
discussed above, in August 2023, we acquired the underlying intellectual property of, as well as the rights to manufacture and sell,
CellerateRX Surgical and HYCOL products from Applied. In connection with this acquisition, Applied assigned its license agreement
with CGI Cellerate RX to a wholly owned subsidiary of the Company and no further royalties will be due to Applied
thereunder. Since the Closing of the Applied Asset Purchase, Sanara indirectly makes intercompany royalty payments to SMAT at
the same rate as set forth in the Sublicense Agreement. These intercompany royalty payments and the offsetting cost of goods sold were
eliminated in consolidation effective as of August 1, 2023.
Consulting
Agreement
In
July 2021, we entered into an asset purchase agreement with Rochal, a related party. Concurrent with the Rochal asset purchase, we entered
into a consulting agreement with Ann Beal Salamone pursuant to which Ms. Salamone agreed to provide us with consulting services with
respect to, among other things, writing new patents, conducting patent intelligence and participating in certain grant and contract reporting.
In consideration for the consulting services to be provided to us, Ms. Salamone is entitled to receive an annual consulting fee of $177,697,
with payments to be paid once per month. The consulting agreement has an initial term of three years, unless earlier terminated by us,
and is subject to renewal. Ms. Salamone is a director of the Company, is a significant shareholder and the current Chair of the board
of directors of Rochal.
Catalyst
Transaction Advisory Services Agreement
In
March 2023, we entered into a Transaction Advisory Services Agreement (the “Catalyst Services Agreement”) effective March
1, 2023 with Catalyst, a related party. Pursuant to the Catalyst Services Agreement, Catalyst, by and through its directors, officers,
employees and affiliates that are not simultaneously serving as directors, officers or employees of the Company (collectively, the “Covered
Persons”), agreed to perform certain transaction advisory, business and organizational strategy, finance, marketing, operational
and strategic planning, relationship access and corporate development services for us in connection with any merger, acquisition, recapitalization,
divestiture, financing, refinancing, or other similar transaction in which we may be, or may consider becoming, involved, and any such
additional services as mutually agreed upon in writing by and between Catalyst and us (the “Catalyst Services”).
Pursuant
to the Catalyst Services Agreement, we agreed to reimburse Catalyst for (i) compensation actually paid by Catalyst to any of the
Covered Persons at a rate no more than a rate consistent with industry practice for the performance of services similar to the
Catalyst Services, as documented in reasonably sufficient detail, and (ii) all reasonable out-of-pocket costs and expenses payable
to unaffiliated third parties, as documented in customary expense reports, as each of (i) and (ii) is incurred in connection with
the Catalyst Services rendered under the Catalyst Services Agreement, with all reimbursements being contingent upon the prior
approval of the Audit Committee of our Board of Directors. We incurred $44,032 and $117,018 of costs pursuant to the Catalyst
Services Agreement during the three and nine months ended September 30, 2023.
Receivables
and Payables
We
had outstanding related party receivables totaling $11,032 at September 30, 2023, and $98,548 at December 31, 2022. We had outstanding
related party payables totaling $64,747 at September 30, 2023, and $34,036 at December 31, 2022.
IMPACT
OF INFLATION AND CHANGING PRICES
Inflation
and changing prices have not had a material impact on our historical results of operations. We do not currently anticipate that inflation
and changing prices will have a material impact on our future results of operations.
CRITICAL
ACCOUNTING ESTIMATES
The
preparation of financial statements in accordance with U.S. generally accepted accounting principles requires management to make estimates
and assumptions that affect the amounts reported in the unaudited consolidated financial statements and accompanying notes. Although
we base our estimates on historical experience and various other assumptions that we believe to be reasonable under the circumstances,
actual results may differ from the estimates on which our financial statements are prepared at any given point of time. Changes in these
estimates could materially affect our consolidated financial position, results of operations or cash flows. Significant items that are
subject to such estimates and assumptions include revenue and expense accruals, the fair value measurement of assets and liabilities
and the allocation of purchase price to the fair value of assets acquired. Our critical accounting estimates have not significantly changed
since December 31, 2022 and are disclosed in our Annual Report on Form 10-K for the year ended December 31, 2022.
ITEM
3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
As
a smaller reporting company, we are not required to provide this information.
ITEM
4. CONTROLS AND PROCEDURES
EVALUATION
OF DISCLOSURE CONTROLS AND PROCEDURES
We
maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed by us in the reports
that we file or submit to the Securities and Exchange Commission (the “SEC”) under the Securities Exchange Act of 1934, as
amended (the “Exchange Act”), is recorded, processed, summarized and reported within the time periods specified by the SEC’s
rules and forms, and that information is accumulated and communicated to our management, including our principal executive and principal
financial officers (whom we refer to in this periodic report as our Certifying Officers), as appropriate to allow timely decisions regarding
required disclosure. Our management evaluated, with the participation of our Certifying Officers, the effectiveness of our disclosure
controls and procedures as of September 30, 2023, pursuant to Rule 13a-15(b) under the Exchange Act. Based upon that evaluation, our
Certifying Officers concluded that, as of September 30, 2023, our disclosure controls and procedures were effective.
CHANGES
IN INTERNAL CONTROL OVER FINANCIAL REPORTING
There
were no changes in our internal control over financial reporting that occurred during the quarter ended September 30, 2023 that have
materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
Part
II — Other Information
ITEM
1. LEGAL PROCEEDINGS
From
time to time, we may be involved in claims and legal actions that arise in the ordinary course of business. To our knowledge, there are
no material pending legal proceedings to which we are a party or of which any of our property is the subject.
ITEM
1A. RISK FACTORS
Except
as provided below, there were no material changes to the Risk Factors disclosed in “Item 1A. Risk Factors” in our Annual
Report on Form 10-K for the year ended December 31, 2022. For more information concerning our risk factors, please see “Item 1A.
Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022.
We
may fail to realize all the anticipated benefits of the Applied Asset Purchase, or such benefits may take longer to realize than expected.
We
may fail to realize all of the anticipated benefits of the Applied Asset Purchase, including expected operational, research and development
and cost synergies, or such benefits may not be achieved within the anticipated timeframe. In addition, in connection with the Applied
Asset Purchase, we acquired control of the manufacturing of our CellerateRX Surgical and HYCOL products, which was previously controlled
by the Sellers. If we are unable to maintain or replace the Sellers’ manufacturing process, our sales of CellerateRX Surgical and
HYCOL products could be jeopardized.
Furthermore,
we have incurred significant transaction costs in connection with the Applied Asset Purchase, including payment of certain fees and expenses
incurred in connection with the Applied Asset Purchase and the financing of the Applied Asset Purchase, and our future financial results
could be impacted if the intangible assets we acquired in the Applied Asset Purchase become impaired. The failure to realize the anticipated
benefits of the Applied Asset Purchase or any of our other recent acquisitions could cause an interruption of, or a loss of momentum
in, our operations and could result in a material adverse effect on our financial condition, results of operations or cash flows.
Our
indebtedness could adversely affect our financial condition and prevent us from fulfilling our obligations.
A
significant portion of our future cash flow is required to pay interest and principal on our outstanding indebtedness, and we may be
unable to generate sufficient cash flow from operations, or have future borrowings available, to enable us to repay our indebtedness
or to fund other liquidity needs. Among other consequences, this indebtedness could:
● |
require
us to use a significant percentage of our cash flow from operations for debt service and the satisfaction of repayment obligations,
and not for other purposes, such as funding working capital and capital expenditures or making future acquisitions; |
● |
cause
our interest expense to increase if there is a general increase in interest rates, because a portion of our indebtedness bears interest
at floating rates; |
● |
limit
our flexibility in planning for or reacting to changes in our business and limit our ability to exploit future business opportunities;
and |
● |
cause
us to be more highly leveraged than some of our competitors, which may place us at a competitive disadvantage. |
Our
outstanding indebtedness is subject to certain operating and financial covenants that restrict our business and financing activities
and may adversely affect our cash flow and our ability to operate our business.
The
Loan Agreement requires us and SMAT, to maintain compliance with certain operating and financial covenants, which provide that we or
SMAT, among other things, may not, subject to certain exceptions:
● |
create
or permit the existence of additional liens on our assets; |
● |
enter
into any pledge agreements or arrangements; |
● |
with
respect to SMAT, make investments in or provide capital contributions to other entities; |
● |
enter
into a merger or consolidation or acquire any assets outside of the ordinary course of business; |
● |
dispose
of a material part of our assets or property or enter into any sale-leaseback transactions; |
● |
with
respect to SMAT, pay dividends or distributions of our capital stock, without the prior written consent of the Bank; |
● |
make
or permit to remain outstanding any loans; |
● |
change
the nature of our business; |
● |
enter
into transactions with affiliates other than in the ordinary course of business on an arm’s-length basis; or |
● |
amend,
modify or obtain or grant a waiver of any provision of any document or instrument evidencing or securing any of our subordinated
indebtedness. |
In
addition, starting with the quarter ending September 30, 2023, SMAT is required to maintain a minimum Debt Service Coverage Ratio of
1.2 to 1.0, which ratio is calculated as of the last day of the applicable fiscal quarter. SMAT is also required to maintain as of the
end of each fiscal quarter a maximum Cash Flow Leverage Ratio of not more than (a) 4.5 to 1.0 as of the last day of the fiscal quarter
ending on September 30, 2023, (b) 4.0 to 1.0 as of the last day of each fiscal quarter ending on December 31, 2023, and March 31, 2024,
(c) 3.5 to 1.0 as of the last day of each fiscal quarter ending on June 30, 2024, and September 30, 2024, and (d) 3.0 to 1.0 as of the
last day of each fiscal quarter thereafter.
Further, in the event that SMAT fails to comply
with its financial covenants, we are required to contribute cash to SMAT in an amount equal to the amount required to satisfy the financial
covenants. During the three months ended September 30, 2023, we contributed an immaterial amount of cash to SMAT to ensure that SMAT
was in compliance with the financial covenants under the Loan Agreement as of September 30, 2023. If we are required to make additional
cash contributions to SMAT in future periods, we may not have sufficient funds available to fulfill such obligation.
A
breach of any of the covenants under our loan agreements, subject to certain cure periods, will result in an event of default, which
could cause all of our outstanding indebtedness under the Loan Agreement to become immediately due and payable, and a default interest
rate of an additional 5.0% per annum may be applied to the outstanding loan balance. If our indebtedness is accelerated, we cannot be
certain that we will have sufficient funds available to pay the accelerated indebtedness or that we will have the ability to refinance
the accelerated indebtedness on terms favorable to us or at all.
As
a result of the negative covenants contained in the Loan Agreement and the need for cash to pay interest and principal amortization payments
required under the Loan Agreement, the Company may not have access to cash it otherwise would have for working capital, capital expenditures,
acquisitions, general corporate purposes or other purposes.
Pursuant
to the Loan Agreement, SMAT is subject to restrictions on making certain payments, including dividends, other distributions and loans,
to the Company. As a result, although SMAT may use its cash to repay the Term Loan, the Company may not have access to cash it otherwise
would have for working capital, capital expenditures, acquisitions, general corporate purposes or other purposes.
If
our Executive Chairman ceases to serve as the Chairman of the Board of Directors of the Company or SMAT, such event could result in an
event of default under the Loan Agreement.
The
Loan Agreement provides that if Ron Nixon, our Executive Chairman, ceases to serve as Chairman of the Board of Directors of the Company
or SMAT, an event of default will occur under the Loan Agreement, unless a successor, acceptable to the Bank, is elected or appointed
within 10 business days of such event. If such an event were to occur and we are unable to find a replacement suitable to the Bank, we
would be in default and all of our outstanding indebtedness could become immediately due and payable, and a default interest rate of
an additional 5.0% per annum may be applied to the outstanding loan balance.
ITEM
2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
There
were no sales of unregistered securities during the quarter ended September 30, 2023 that were not previously reported on a Current Report
on Form 8-K.
ITEM
3. DEFAULTS UPON SENIOR SECURITIES
None.
ITEM
4. MINE SAFETY DISCLOSURES
This
item is not applicable.
ITEM
5. OTHER INFORMATION
None.
ITEM
6. EXHIBITS
The
exhibits listed below are filed as part of this Report or incorporated herein by reference.
Exhibit
No. |
|
Description |
|
|
|
2.1# |
|
Asset Purchase Agreement, dated July 14, 2021, by and between Sanara MedTech Inc., as Purchaser, and Rochal Industries, LLC, as Seller (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on July 19, 2021). |
|
|
|
2.2# |
|
Agreement and Plan of Merger, dated April 1, 2022, by and among Sanara MedTech Inc., United Wound and Skin Solutions, LLC, Precision Healing Inc., PH Merger Sub I, Inc., PH Merger Sub II, LLC and Furneaux Capital Holdco, LLC (d/b/a BlueIO) (incorporated by reference to Exhibit 2.1 to the Company’s Current Report on Form 8-K filed on April 4, 2022). |
|
|
|
2.3# |
|
Membership Interest Purchase Agreement, dated July 1, 2022, by and among Sanara MedTech Inc., Scendia Biologics, LLC and Ryan Phillips (incorporated by reference to Exhibit 2.1 to the Company’s Current Report on Form 8-K filed on July 5, 2022). |
|
|
|
2.4# |
|
Asset Purchase Agreement dated, August 1, 2023, by and among Sanara MedTech Inc., Sanara MedTech Applied Technologies, LLC, The Hymed Group Corporation, Applied Nutritionals, LLC and Dr. George D. Petito (incorporated by reference to Exhibit 2.1 to the Company’s Current Report on Form 8-K filed on August 2, 2023). |
|
|
|
3.1 |
|
Articles of Incorporation of Sanara MedTech Inc. (as amended through December 30, 2020) (incorporated by reference to Exhibit 3.1 to the Company’s Annual Report on Form 10-K filed on March 30, 2021). |
|
|
|
3.2 |
|
Bylaws (incorporated by reference to Exhibit 3.2 to the Company’s Registration Statement on Form S-1 filed April 11, 2008). |
|
|
|
10.1+ |
|
Professional Services Agreement, dated August 1, 2023, by and between Sanara MedTech Inc. and Dr. George D. Petito (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on August 2, 2023). |
|
|
|
10.2+ |
|
Loan Agreement, dated August 1, 2023, between Sanara MedTech Applied Technologies, LLC, Sanara MedTech Inc. and Cadence Bank (incorporated by reference to Exhibit 10.2 to the Company’s Current Report on Form 8-K filed on August 2, 2023). |
|
|
|
31.1* |
|
Certification of Principal Executive Officer in accordance with 18 U.S.C. Section 1350, as adopted by Section 302 of the Sarbanes-Oxley Act of 2002. |
|
|
|
31.2* |
|
Certification of Principal Financial Officer in accordance with 18 U.S.C. Section 1350, as adopted by Section 302 of the Sarbanes-Oxley Act of 2002. |
|
|
|
32.1** |
|
Certification of Principal Executive Officer in accordance with 18 U.S.C. Section 1350, as adopted by Section 906 of the Sarbanes-Oxley Act of 2002. |
|
|
|
32.2** |
|
Certification of Principal Financial Officer in accordance with 18 U.S.C. Section 1350, as adopted by Section 906 of the Sarbanes-Oxley Act of 2002.
|
101.INS |
|
Inline
XBRL Instance Document. |
101.SCH |
|
Inline
XBRL Taxonomy Extension Schema Document. |
101.CAL |
|
Inline
XBRL Taxonomy Extension Calculation Linkbase Document. |
101.DEF |
|
Inline
XBRL Taxonomy Extension Definition Linkbase Document. |
101.LAB |
|
Inline
XBRL Taxonomy Extension Label Linkbase Document. |
101.PRE |
|
Inline
XBRL Taxonomy Extension Presentation Linkbase Document. |
104 |
|
Cover
Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101). |
*
Filed herewith
**
The certifications attached as Exhibit 32.1 and Exhibit 32.2 are not deemed “filed” with the Securities and Exchange Commission
and are not to be incorporated by reference into any filing of Sanara MedTech Inc. under the Securities Act of 1933, as amended, or the
Securities Exchange Act of 1934, as amended, whether made before or after the date of this Quarterly Report on Form 10-Q, irrespective
of any general incorporation language contained in such filing.
#
Certain schedules and exhibits to this agreement have been omitted pursuant to Item 601(a)(5) of Regulation S-K. A copy of any omitted
schedule or exhibit will be furnished supplementally to the Securities and Exchange Commission or its staff upon request. If indicated
on the first page of such agreement, certain confidential information has been excluded pursuant to Item 601(b)(2)(ii) of Regulation
S-K. Such excluded information is not material and is the type that the Company treats as private or confidential.
+
Certain schedules and exhibits to this agreement have been omitted pursuant to Item 601(a)(5) of Regulation S-K. A copy of any omitted
schedule or exhibit will be furnished supplementally to the Securities and Exchange Commission or its staff upon request. Certain confidential
information has been excluded pursuant to Item 601(b)(10)(iv) of Regulation S-K. Such excluded information is not material and is the
type that the Company treats as private or confidential.
SIGNATURES
Pursuant
to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed
on its behalf by the undersigned, thereunto duly authorized.
|
SANARA MEDTECH INC. |
|
|
|
November
13, 2023 |
By: |
/s/
Michael D. McNeil |
|
|
Michael
D. McNeil |
|
|
Chief
Financial Officer |
|
|
(Principal
Financial Officer and duly authorized officer) |
|
|
|
EXHIBIT 31.1
CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER
IN ACCORDANCE WITH 18 U.S.C. SECTION 1350,
AS ADOPTED BY SECTION 302 OF THE SARBANES-OXLEY
ACT OF 2002
I, Zachary B. Fleming, certify that:
1. |
I have reviewed this Quarterly Report on Form 10-Q of Sanara MedTech Inc. for the period ended September 30, 2023; |
|
|
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
|
|
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
|
|
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
(a) |
|
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
|
|
|
(b) |
|
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
|
|
|
(c) |
|
Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
|
|
|
(d) |
|
Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
(a) |
|
All significant deficiencies and material weaknesses in the design or operation of internal controls over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
|
|
|
(b) |
|
Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
Date: November 13, 2023
/s/ Zachary B. Fleming |
|
Zachary B. Fleming, Chief Executive Officer |
|
EXHIBIT 31.2
CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER
IN ACCORDANCE WITH 18 U.S.C. SECTION 1350,
AS ADOPTED BY SECTION 302 OF THE SARBANES-OXLEY
ACT OF 2002
I, Michael D. McNeil, certify that:
1. |
I have reviewed this Quarterly Report on Form 10-Q of Sanara MedTech Inc. for the period ended September 30, 2023; |
|
|
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
|
|
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
|
|
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
(a) |
|
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
|
|
|
(b) |
|
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
|
|
|
(c) |
|
Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
|
|
|
(d) |
|
Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
(a) |
|
All significant deficiencies and material weaknesses in the design or operation of internal controls over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
|
|
|
(b) |
|
Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
Date: November 13, 2023
/s/ Michael D. McNeil |
|
Michael D. McNeil, Chief Financial Officer |
|
EXHIBIT 32.1
CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER
IN ACCORDANCE WITH 18 U.S.C. SECTION 1350,
AS ADOPTED BY SECTION 906 OF THE SARBANES-OXLEY
ACT OF 2002
In connection with the Quarterly Report on Form 10-Q
of Sanara MedTech Inc. (the “Company”) for the period ended September 30, 2023 as filed with the Securities and Exchange Commission
on the date hereof (the “Report”), I, Zachary B. Fleming, in my capacity as Chief Executive Officer of the Company and not
in my individual capacity, certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of
2002, that to my knowledge:
|
(1) |
The Report fully complies with the requirements of section 13(a) or 15(d), as applicable, of the Securities Exchange Act of 1934; and |
|
(2) |
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company as of, and for, the periods presented in the Report. |
Date: November 13, 2023
/s/ Zachary B. Fleming |
|
Zachary B. Fleming, Chief Executive Officer |
|
The foregoing certification is being furnished as
an exhibit to the Report pursuant to Item 601(b)(32) of Regulation S-K and Section 906 of the Sarbanes-Oxley Act of 2002 (subsections
(a) and (b) of Section 1350, Chapter 63 of Title 18, United States Code) and, accordingly, is not being filed as part of the Report for
purposes of Section 18 of the Securities Exchange Act of 1934, as amended, and is not incorporated by reference into any filing of the
Company, whether made before or after the date hereof, regardless of any general incorporation language in such filing.
EXHIBIT 32.2
CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER
IN ACCORDANCE WITH 18 U.S.C. SECTION 1350,
AS ADOPTED BY SECTION 906 OF THE SARBANES-OXLEY
ACT OF 2002
In connection with the Quarterly Report on Form 10-Q
of Sanara MedTech Inc. (the “Company”) for the period ended September 30, 2023 as filed with the Securities and Exchange Commission
on the date hereof (the “Report”), I, Michael D. McNeil, in my capacity as Chief Financial Officer of the Company and not
in my individual capacity, certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of
2002, that to my knowledge:
|
(1) |
The Report fully complies with the requirements of section 13(a) or 15(d), as applicable, of the Securities Exchange Act of 1934; and |
|
(2) |
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company as of, and for, the periods presented in the Report. |
November 13, 2023
/s/
Michael D. McNeil |
|
Michael D. McNeil, Chief Financial Officer |
|
The foregoing certification is being furnished as
an exhibit to the Report pursuant to Item 601(b)(32) of Regulation S-K and Section 906 of the Sarbanes-Oxley Act of 2002 (subsections
(a) and (b) of Section 1350, Chapter 63 of Title 18, United States Code) and, accordingly, is not being filed as part of the Report for
purposes of Section 18 of the Securities Exchange Act of 1934, as amended, and is not incorporated by reference into any filing of the
Company, whether made before or after the date hereof, regardless of any general incorporation language in such filing.
v3.23.3
Cover - shares
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Sep. 30, 2023 |
Nov. 13, 2023 |
Cover [Abstract] |
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|
|
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--12-31
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Entity File Number |
001-39678
|
|
Entity Registrant Name |
SANARA
MEDTECH INC.
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Entity Central Index Key |
0000714256
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v3.23.3
Consolidated Balance Sheets - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Current assets |
|
|
Cash |
$ 6,235,912
|
$ 8,958,995
|
Royalty receivable |
49,344
|
99,594
|
Inventory, net |
5,021,030
|
3,549,000
|
Prepaid and other assets |
621,690
|
1,104,611
|
Total current assets |
19,375,303
|
20,616,509
|
Long-term assets |
|
|
Property and equipment, net |
1,327,056
|
1,416,436
|
Right of use assets – operating leases |
2,094,188
|
806,402
|
Goodwill |
3,601,781
|
3,601,781
|
Intangible assets, net |
45,991,466
|
31,509,980
|
Investment in equity securities |
3,084,278
|
3,084,278
|
Total long-term assets |
56,098,769
|
40,418,877
|
Total assets |
75,474,072
|
61,035,386
|
Current liabilities |
|
|
Accrued royalties and expenses |
3,583,439
|
2,144,475
|
Accrued bonuses and commissions |
6,084,654
|
7,758,284
|
Earnout liabilities – current |
1,000,000
|
1,162,880
|
Operating lease liabilities – current |
322,206
|
313,933
|
Current portion of debt |
232,143
|
|
Total current liabilities |
13,227,076
|
12,806,309
|
Long-term liabilities |
|
|
Earnout liabilities – long-term |
4,871,986
|
6,003,811
|
Operating lease liabilities – long-term |
1,846,293
|
505,291
|
Long-term debt, net of current portion |
9,458,254
|
|
Other long-term liabilities |
1,972,673
|
|
Total long-term liabilities |
18,149,206
|
6,509,102
|
Total liabilities |
31,376,282
|
19,315,411
|
Commitments and contingencies (Note 10) |
|
|
Shareholders’ equity |
|
|
Common Stock: $0.001 par value, 20,000,000 shares authorized; 8,540,226 issued and outstanding as of September 30, 2023 and 8,299,957 issued and outstanding as of December 31, 2022 |
8,540
|
8,300
|
Additional paid-in capital |
72,107,881
|
65,213,987
|
Accumulated deficit |
(27,799,621)
|
(23,394,757)
|
Total Sanara MedTech shareholders’ equity |
44,316,800
|
41,827,530
|
Equity attributable to noncontrolling interest |
(219,010)
|
(107,555)
|
Total shareholders’ equity |
44,097,790
|
41,719,975
|
Total liabilities and shareholders’ equity |
75,474,072
|
61,035,386
|
Nonrelated Party [Member] |
|
|
Current assets |
|
|
Accounts receivable |
7,436,295
|
6,805,761
|
Current liabilities |
|
|
Accounts payable |
1,939,887
|
1,392,701
|
Related Party [Member] |
|
|
Current assets |
|
|
Accounts receivable |
11,032
|
98,548
|
Current liabilities |
|
|
Accounts payable |
$ 64,747
|
$ 34,036
|
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v3.23.3
Consolidated Balance Sheets (Parenthetical) - $ / shares
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Statement of Financial Position [Abstract] |
|
|
Common stock, par value |
$ 0.001
|
$ 0.001
|
Common stock, shares authorized |
20,000,000
|
20,000,000
|
Common stock, shares issued |
8,540,226
|
8,299,957
|
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8,540,226
|
8,299,957
|
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v3.23.3
Consolidated Statements of Operations (Unaudited) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Income Statement [Abstract] |
|
|
|
|
Net Revenue |
$ 16,024,948
|
$ 13,044,571
|
$ 47,300,029
|
$ 30,526,572
|
Cost of goods sold |
1,751,349
|
2,228,561
|
6,064,524
|
3,991,728
|
Gross profit |
14,273,599
|
10,816,010
|
41,235,505
|
26,534,844
|
Operating expenses |
|
|
|
|
Selling, general and administrative expenses |
13,877,879
|
12,062,195
|
40,658,424
|
31,865,958
|
Research and development |
986,454
|
1,061,387
|
3,480,906
|
2,333,024
|
Depreciation and amortization |
997,674
|
814,881
|
2,580,243
|
1,556,752
|
Change in fair value of earnout liabilities |
(681,753)
|
109,689
|
(1,494,910)
|
173,116
|
Total operating expenses |
15,180,254
|
14,048,152
|
45,224,663
|
35,928,850
|
Operating loss |
(906,655)
|
(3,232,142)
|
(3,989,158)
|
(9,394,006)
|
Other expense |
|
|
|
|
Interest expense and other |
(188,294)
|
|
(188,300)
|
|
Share of losses from equity method investment |
|
|
|
(379,633)
|
Total other expense |
(188,294)
|
|
(188,300)
|
(379,633)
|
Loss before income taxes |
(1,094,949)
|
(3,232,142)
|
(4,177,458)
|
(9,773,639)
|
Income tax benefit |
|
1,702,890
|
|
5,844,796
|
Net loss |
(1,094,949)
|
(1,529,252)
|
(4,177,458)
|
(3,928,843)
|
Less: Net loss attributable to noncontrolling interest |
(34,579)
|
(58,792)
|
(111,455)
|
(98,485)
|
Net loss attributable to Sanara MedTech shareholders |
$ (1,060,370)
|
$ (1,470,460)
|
$ (4,066,003)
|
$ (3,830,358)
|
Net loss per share of common stock, basic |
$ (0.13)
|
$ (0.18)
|
$ (0.49)
|
$ (0.49)
|
Net loss per share of common stock, diluted |
$ (0.13)
|
$ (0.18)
|
$ (0.49)
|
$ (0.49)
|
Weighted average number of common shares outstanding, basic |
8,332,341
|
8,107,261
|
8,244,503
|
7,836,882
|
Weighted average number of common shares outstanding, diluted |
8,332,341
|
8,107,261
|
8,244,503
|
7,836,882
|
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v3.23.3
Consolidated Statements of Changes in Shareholders' Equity (Unaudited) - USD ($)
|
Common Stock [Member] |
Additional Paid-in Capital [Member] |
Retained Earnings [Member] |
Noncontrolling Interest [Member] |
Total |
Balance at Dec. 31, 2021 |
$ 7,677
|
$ 45,867,768
|
$ (15,235,044)
|
$ (488,397)
|
$ 30,152,004
|
Balance, shares at Dec. 31, 2021 |
7,676,662
|
|
|
|
|
Share-based compensation |
$ 136
|
1,622,982
|
|
|
1,623,118
|
Share-based compensation, shares |
137,076
|
|
|
|
|
Net settlement and retirement of equity-based awards |
$ (3)
|
(52,284)
|
(50,644)
|
|
(102,931)
|
Net settlement and retirement of equity-based awards, shares |
(3,343)
|
|
|
|
|
Net income (loss) |
|
|
(3,129,324)
|
(27,181)
|
(3,156,505)
|
Balance at Mar. 31, 2022 |
$ 7,810
|
47,438,466
|
(18,415,012)
|
(515,578)
|
28,515,686
|
Balance, shares at Mar. 31, 2022 |
7,810,395
|
|
|
|
|
Balance at Dec. 31, 2021 |
$ 7,677
|
45,867,768
|
(15,235,044)
|
(488,397)
|
30,152,004
|
Balance, shares at Dec. 31, 2021 |
7,676,662
|
|
|
|
|
Net income (loss) |
|
|
|
|
(3,928,843)
|
Balance at Sep. 30, 2022 |
$ 8,304
|
64,565,730
|
(19,116,046)
|
(809,520)
|
44,648,468
|
Balance, shares at Sep. 30, 2022 |
8,303,729
|
|
|
|
|
Balance at Mar. 31, 2022 |
$ 7,810
|
47,438,466
|
(18,415,012)
|
(515,578)
|
28,515,686
|
Balance, shares at Mar. 31, 2022 |
7,810,395
|
|
|
|
|
Share-based compensation |
$ 39
|
703,361
|
|
|
703,400
|
Share-based compensation, shares |
39,268
|
|
|
|
|
Net income (loss) |
|
|
769,426
|
(12,512)
|
756,914
|
Issuance of common stock for acquisitions |
$ 166
|
5,096,278
|
|
|
5,096,444
|
Issuance of common stock for acquisitions, shares |
165,738
|
|
|
|
|
Issuance of common stock options and warrants for acquisitions |
|
4,612,645
|
|
|
4,612,645
|
Distribution to noncontrolling interest member |
|
|
|
(220,000)
|
(220,000)
|
Balance at Jun. 30, 2022 |
$ 8,015
|
57,850,750
|
(17,645,586)
|
(748,090)
|
39,465,089
|
Balance, shares at Jun. 30, 2022 |
8,015,401
|
|
|
|
|
Share-based compensation |
$ (3)
|
683,205
|
|
|
683,202
|
Share-based compensation, shares |
(3,358)
|
|
|
|
|
Net income (loss) |
|
|
(1,470,460)
|
(58,792)
|
(1,529,252)
|
Issuance of common stock for acquisitions |
$ 292
|
6,031,775
|
|
(2,638)
|
6,029,429
|
Issuance of common stock for acquisitions, shares |
291,686
|
|
|
|
|
Balance at Sep. 30, 2022 |
$ 8,304
|
64,565,730
|
(19,116,046)
|
(809,520)
|
44,648,468
|
Balance, shares at Sep. 30, 2022 |
8,303,729
|
|
|
|
|
Balance at Dec. 31, 2022 |
$ 8,300
|
65,213,987
|
(23,394,757)
|
(107,555)
|
41,719,975
|
Balance, shares at Dec. 31, 2022 |
8,299,957
|
|
|
|
|
Share-based compensation |
$ 75
|
597,230
|
|
|
597,305
|
Share-based compensation, shares |
74,781
|
|
|
|
|
Net settlement and retirement of equity-based awards |
$ (16)
|
(315,572)
|
(340,354)
|
|
(655,942)
|
Net settlement and retirement of equity-based awards, shares |
(15,854)
|
|
|
|
|
Net income (loss) |
|
|
(1,177,900)
|
(38,429)
|
(1,216,329)
|
Issuance of common stock in equity offering |
$ 26
|
1,033,735
|
|
|
1,033,761
|
Issuance of common stock in equity offering, shares |
26,143
|
|
|
|
|
Balance at Mar. 31, 2023 |
$ 8,385
|
66,529,380
|
(24,913,011)
|
(145,984)
|
41,478,770
|
Balance, shares at Mar. 31, 2023 |
8,385,027
|
|
|
|
|
Balance at Dec. 31, 2022 |
$ 8,300
|
65,213,987
|
(23,394,757)
|
(107,555)
|
41,719,975
|
Balance, shares at Dec. 31, 2022 |
8,299,957
|
|
|
|
|
Net income (loss) |
|
|
|
|
(4,177,458)
|
Balance at Sep. 30, 2023 |
$ 8,540
|
72,107,881
|
(27,799,621)
|
(219,010)
|
44,097,790
|
Balance, shares at Sep. 30, 2023 |
8,540,226
|
|
|
|
|
Balance at Mar. 31, 2023 |
$ 8,385
|
66,529,380
|
(24,913,011)
|
(145,984)
|
41,478,770
|
Balance, shares at Mar. 31, 2023 |
8,385,027
|
|
|
|
|
Share-based compensation |
$ 33
|
1,127,299
|
|
|
1,127,332
|
Share-based compensation, shares |
33,355
|
|
|
|
|
Net settlement and retirement of equity-based awards |
$ 22
|
224,740
|
(186)
|
|
224,576
|
Net settlement and retirement of equity-based awards, shares |
21,363
|
|
|
|
|
Net income (loss) |
|
|
(1,827,733)
|
(38,447)
|
(1,866,180)
|
Balance at Jun. 30, 2023 |
$ 8,440
|
67,881,419
|
(26,740,930)
|
(184,431)
|
40,964,498
|
Balance, shares at Jun. 30, 2023 |
8,439,745
|
|
|
|
|
Share-based compensation |
$ (1)
|
857,527
|
|
|
857,526
|
Share-based compensation, shares |
(339)
|
|
|
|
|
Net settlement and retirement of equity-based awards |
$ 27
|
279,364
|
1,679
|
|
281,070
|
Net settlement and retirement of equity-based awards, shares |
27,011
|
|
|
|
|
Net income (loss) |
|
|
(1,060,370)
|
(34,579)
|
(1,094,949)
|
Issuance of common stock for acquisitions |
$ 74
|
3,089,571
|
|
|
3,089,645
|
Issuance of common stock for acquisitions, shares |
73,809
|
|
|
|
|
Balance at Sep. 30, 2023 |
$ 8,540
|
$ 72,107,881
|
$ (27,799,621)
|
$ (219,010)
|
$ 44,097,790
|
Balance, shares at Sep. 30, 2023 |
8,540,226
|
|
|
|
|
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v3.23.3
Consolidated Statements of Cash Flows (Unaudited) - USD ($)
|
9 Months Ended |
Sep. 30, 2023 |
Sep. 30, 2022 |
Cash flows from operating activities: |
|
|
Net loss |
$ (4,177,458)
|
$ (3,928,843)
|
Adjustments to reconcile net loss to net cash used in operating activities: |
|
|
Depreciation and amortization |
2,580,243
|
1,556,752
|
Loss on disposal of property and equipment |
|
2,876
|
Bad debt expense |
214,061
|
220,000
|
Inventory obsolescence |
222,691
|
289,406
|
Share-based compensation |
2,582,163
|
1,971,537
|
Noncash lease expense |
243,988
|
189,409
|
Loss on equity method investment |
|
379,633
|
Benefit from deferred income taxes |
|
(5,844,796)
|
Accretion of finance liabilities |
39,699
|
|
Amortization of debt issuance costs |
2,055
|
(0)
|
Change in fair value of earnout liabilities |
(1,494,910)
|
173,116
|
Changes in operating assets and liabilities: |
|
|
Accounts receivable, net |
(794,344)
|
(754,934)
|
Accounts receivable – related party |
87,516
|
10,920
|
Inventory, net |
(1,664,714)
|
(451,838)
|
Prepaid and other assets |
482,921
|
(69,490)
|
Accounts payable |
547,186
|
(800,788)
|
Accounts payable – related parties |
30,711
|
(126,812)
|
Accrued royalties and expenses |
557,295
|
947,130
|
Accrued bonuses and commissions |
(1,673,629)
|
1,516,858
|
Operating lease liabilities |
(182,498)
|
(189,990)
|
Net cash used in operating activities |
(2,397,024)
|
(4,909,854)
|
Cash flows from investing activities: |
|
|
Purchases of property and equipment |
(210,970)
|
(93,651)
|
Proceeds from disposal of property and equipment |
650
|
894
|
Purchases of intangible assets |
|
(600,000)
|
Investment in equity securities |
|
(250,000)
|
Acquisitions, net of cash acquired |
(9,942,750)
|
(2,191,919)
|
Net cash used in investing activities |
(10,153,070)
|
(3,134,676)
|
Cash flows from financing activities: |
|
|
Loan proceeds, net |
9,688,341
|
|
Equity offering net proceeds |
1,033,761
|
|
Net settlement of equity-based awards |
(150,296)
|
(102,931)
|
Cash payment of finance and earnout liabilities |
(744,795)
|
|
Distribution to noncontrolling interest member |
|
(220,000)
|
Net cash provided by (used in) financing activities |
9,827,011
|
(322,931)
|
Net decrease in cash |
(2,723,083)
|
(8,367,461)
|
Cash, beginning of period |
8,958,995
|
18,652,841
|
Cash, end of period |
6,235,912
|
10,285,380
|
Cash paid during the period for: |
|
|
Interest |
146,546
|
|
Supplemental noncash investing and financing activities: |
|
|
Right of use assets obtained in exchange for lease obligations |
1,531,773
|
|
Equity issued for acquisitions |
3,089,645
|
15,738,518
|
Earnout and other liabilities generated by acquisitions |
3,759,642
|
6,882,151
|
Investment in equity securities converted in asset acquisition |
|
$ 1,803,440
|
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v3.23.3
NATURE OF BUSINESS AND BACKGROUND
|
9 Months Ended |
Sep. 30, 2023 |
Organization, Consolidation and Presentation of Financial Statements [Abstract] |
|
NATURE OF BUSINESS AND BACKGROUND |
NOTE
1 – NATURE OF BUSINESS AND BACKGROUND
Sanara
MedTech Inc. (together with its wholly owned and majority-owned subsidiaries on a consolidated basis, the “Company”) is a
medical technology company focused on developing and commercializing transformative technologies to improve clinical outcomes and reduce
healthcare expenditures in the surgical, chronic wound and skincare markets. Each of the Company’s products, services and technologies
contributes to the Company’s overall goal of achieving better clinical outcomes at a lower overall cost for patients regardless
of where they receive care. The Company strives to be one of the most innovative and comprehensive providers of effective surgical, wound
and skincare solutions and is continually seeking to expand its offerings for patients requiring treatments across the entire continuum
of care in the United States.
|
X |
- DefinitionThe entire disclosure for the nature of an entity's business, major products or services, principal markets including location, and the relative importance of its operations in each business and the basis for the determination, including but not limited to, assets, revenues, or earnings. For an entity that has not commenced principal operations, disclosures about the risks and uncertainties related to the activities in which the entity is currently engaged and an understanding of what those activities are being directed toward.
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v3.23.3
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
|
9 Months Ended |
Sep. 30, 2023 |
Accounting Policies [Abstract] |
|
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES |
NOTE
2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Principles
of Consolidation and Basis of Presentation
The
accompanying unaudited consolidated financial statements include the accounts of Sanara MedTech Inc. and its wholly owned and majority-owned
subsidiaries, as well as other entities in which the Company has a controlling financial interest. All significant intercompany profits,
losses, transactions and balances have been eliminated in consolidation. Certain prior year amounts have been reclassified to conform
to the current year presentation.
The
accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles
for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include
all the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. In the
opinion of management of the Company, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation
have been included. Operating results for interim periods are not necessarily indicative of the results that may be expected for the
full year period. These financial statements and notes should be read in conjunction with the financial statements for each of the two
years ended December 31, 2022 and 2021, which are included in the Company’s most recent Annual Report on Form 10-K.
Use
of Estimates
The
preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates
and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date
of the consolidated financial statements, and the reported revenue and expenses during the reporting period. However, actual results
could differ from those estimates and there may be changes to the Company’s estimates in future periods.
Cash
and Cash Equivalents
The
Company considers all highly liquid investments purchased with an original maturity of three months or less to be cash equivalents.
Income/Loss
Per Share
The
Company computes income/loss per share in accordance with Accounting Standards Codification (“ASC”) Topic 260, Earnings per
Share, which requires the Company to present basic and diluted income per share when the effect is dilutive. Basic income per share is
computed by dividing income available to common shareholders by the weighted average number of shares of common stock outstanding. Diluted
income per share is computed similarly to basic income per share, except that the denominator is increased to include the number of additional
shares of common stock that would have been outstanding if the potential shares of common stock had been issued and if the additional
shares of common stock were dilutive. All common stock equivalents were excluded from the calculations for the periods presented as their
inclusion would have been anti-dilutive during the three and nine months ended September 30, 2023 and 2022 due to the Company’s
net loss.
The
following table summarizes the shares of common stock that were potentially issuable but were excluded from the computation of diluted
net loss per share for the nine months ended September 30, 2023 and 2022, as such shares would have had an anti-dilutive effect:
SCHEDULE
OF COMPUTATION OF DILUTED NET LOSS PER SHARE
| |
2023 | | |
2022 | |
| |
As of September 30, | |
| |
2023 | | |
2022 | |
Stock options (a) | |
| 95,873 | | |
| 155,691 | |
Warrants (b) | |
| 16,725 | | |
| 16,725 | |
Unvested restricted stock | |
| 159,557 | | |
| 192,215 | |
Anti-dilutive securities | |
| 159,557 | | |
| 192,215 | |
(a) | Shares underlying
stock options assumed pursuant to the merger agreement with Precision Healing, Inc. (“Precision Healing”) in April 2022.
See Note 3 for more information regarding the Precision Healing merger. |
(b) | Shares underlying
warrants assumed pursuant to the merger agreement with Precision Healing in April 2022. See Note 3 for more information regarding the
Precision Healing merger. |
Revenue
Recognition
The
Company recognizes revenue in accordance with ASC Topic 606, Revenue from Contracts with Customers (“ASC 606”). Revenues
are recognized when a purchase order is received from the customer and control of the promised goods or services is transferred to the
customer in an amount that reflects the consideration the Company expects to be entitled to receive in exchange for transferring those
goods or services. Revenue is recognized based on the following five-step model:
-
Identification of the contract with a customer
-
Identification of the performance obligations in the contract
-
Determination of the transaction price
-
Allocation of the transaction price to the performance obligations in the contract
-
Recognition of revenue when, or as, the Company satisfies a performance obligation
Details
of this five-step process are as follows:
Identification
of the contract with a customer
Customer
purchase orders are generally considered to be contracts under ASC 606. Purchase orders typically identify the specific terms of products
to be delivered, create the enforceable rights and obligations of both parties and result in commercial substance. No other forms of
contract revenue recognition, such as the completed contract or percentage of completion methods, were utilized by the Company in either
2023 or 2022.
Performance
obligations
The
Company’s performance obligation is generally limited to delivery of the requested items to its customers at the agreed upon quantities
and prices.
Determination
and allocation of the transaction price
The
Company has established prices for its products. These prices are effectively agreed to when customers place purchase orders with the
Company. Rebates and discounts, if any, are recognized in full at the time of sale as a reduction of net revenue. Allocation of transaction
prices is not necessary where only one performance obligation exists.
Recognition
of revenue as performance obligations are satisfied
Product
revenues are recognized when a purchase order is received from the customer, the products are delivered and control of the goods and
services passes to the customer.
Disaggregation
of Revenue
Revenue
streams from product sales and royalties are summarized below for the three and nine months ended September 30, 2023 and 2022.
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Soft tissue repair products | |
$ | 13,634,316 | | |
$ | 10,969,271 | | |
$ | 39,756,539 | | |
$ | 28,296,919 | |
Bone fusion products | |
| 2,340,382 | | |
| 2,025,050 | | |
| 7,392,740 | | |
| 2,078,903 | |
Royalty revenue | |
| 50,250 | | |
| 50,250 | | |
| 150,750 | | |
| 150,750 | |
Total Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
The
Company recognizes royalty revenue from a development and license agreement with BioStructures, LLC. The Company records revenue each
calendar quarter as earned per the terms of the agreement, which stipulates the Company will receive quarterly royalty payments of at
least $50,250. Under the terms of the development and license agreement, royalties of 2.0% are recognized on sales of products containing
the Company’s patented resorbable bone hemostasis. The minimum annual royalty due to the Company is $201,000 per year through the
end of 2023. These royalties are payable in quarterly installments of $50,250. To date, royalties related to this development and license
agreement have not exceeded the annual minimum of $201,000 ($50,250 per quarter).
Accounts
Receivable Allowances
Accounts
receivable are typically due within 30 days of invoicing. The Company establishes an allowance for doubtful accounts to provide for an
estimate of accounts receivable which are not expected to be collectible. The Company bases the allowance on an assessment of customer
creditworthiness, historical payment experience, the age of outstanding receivables and other information as applicable. The Company
recorded bad debt expense of $128,061 and $25,000 during the three months ended September 30, 2023 and 2022, respectively, and $214,061
and $220,000 during the nine months ended September 30, 2023 and 2022, respectively. The allowance for doubtful accounts was $511,089
at September 30, 2023 and $265,089 at December 31, 2022. The Company also establishes other allowances to provide for estimated customer
rebates and other expected customer deductions. These allowances totaled $5,297 at September 30, 2023 and $4,761 at December 31, 2022.
If circumstances related to customers change, estimates of the recoverability of receivables would be further adjusted.
Inventories
Inventories are stated at the lower
of cost or net realizable value, with cost computed on a first-in, first-out basis. Inventories consist primarily of finished goods,
and also include an immaterial amount of raw materials and related packaging components. The Company recorded inventory obsolescence
expense of $152,701
and $129,689
for the three months ended September 30, 2023 and 2022, respectively, and $222,691
and $289,406
for the nine months ended September 30, 2023 and 2022, respectively. The allowance for obsolete and slow-moving inventory had a
balance of $327,492
at September 30, 2023, and $523,832 at
December 31, 2022.
Property
and Equipment
Property
and equipment are stated at cost, less accumulated depreciation. Depreciation is recorded using the straight-line method over the estimated
useful lives of the related assets, ranging from two to ten years. Below is a summary of property and equipment for the periods presented:
SCHEDULE OF PROPERTY AND EQUIPMENT
| |
Useful | | |
September 30, | | |
December 31, | |
| |
Life | | |
2023 | | |
2022 | |
Computers | |
| 3-5 years | | |
$ | 194,788 | | |
$ | 172,154 | |
Office equipment | |
| 3-7 years | | |
| 154,280 | | |
| 87,225 | |
Furniture and fixtures | |
| 5-10 years | | |
| 323,755 | | |
| 258,414 | |
Leasehold improvements | |
| 2-5 years | | |
| 107,983 | | |
| 19,631 | |
Internal use software | |
| 5 years | | |
| 1,618,998 | | |
| 1,618,998 | |
Property and equipment, gross | |
| | | |
| 2,399,804 | | |
| 2,156,422 | |
Less accumulated depreciation | |
| | | |
| (1,072,748 | ) | |
| (739,986 | ) |
Property and equipment, net | |
| | | |
$ | 1,327,056 | | |
$ | 1,416,436 | |
Depreciation
expense related to property and equipment was $116,596 and $106,347 for the three months ended September 30, 2023 and 2022, respectively,
and $332,762 and $300,655 for the nine months ended September 30, 2023 and 2022, respectively.
Internal
Use Software
The
Company accounts for costs incurred to develop or acquire computer software for internal use in accordance with ASC Topic 350-40, Intangibles
– Goodwill and Other. The Company capitalizes the costs incurred during the application development stage, which generally includes
third-party developer fees to design the software configuration and interfaces, coding, installation and testing.
The
Company begins capitalization of qualifying costs when both the preliminary project stage is completed and management has authorized
further funding for the completion of the project. Costs incurred during the preliminary project stage along with post implementation
stages of internal-use computer software are expensed as incurred. The Company also capitalizes costs related to specific upgrades and
enhancements when it is probable the expenditures will result in additional functionality. Capitalized development costs are classified
as “Property and equipment, net” in the Consolidated Balance Sheets and are depreciated over the estimated useful life of the
software, which is generally five years.
Goodwill
The
excess of purchase price over the fair value of identifiable net assets acquired in business combinations is recorded as goodwill. As
of September 30, 2023, all the Company’s goodwill relates to the acquisition of Scendia Biologics, LLC (“Scendia”)
(see Note 4). Goodwill has an indefinite useful life and is not amortized. Goodwill is tested annually as of December 31 for impairment,
or more frequently if circumstances indicate impairment may have occurred. The Company may first perform a qualitative assessment to
determine if it is more likely than not that the fair value of the reporting unit is less than the respective carrying value. If it is
determined that it is more likely than not that a reporting unit’s fair value is less than its carrying value, then the Company
will determine the fair value of the reporting unit and record an impairment charge for the difference between fair value and carrying
value (not to exceed the carrying amount of goodwill). No impairment was recorded during the nine months ended September 30, 2023.
Intangible
Assets
Intangible
assets are stated at cost of acquisition less accumulated amortization and impairment loss, if any. Cost of acquisition includes the
purchase price and any cost directly attributable to bringing the asset to its working condition for the intended use. The Company amortizes
its finite-lived intangible assets on a straight-line basis over the estimated useful life of the respective assets which is generally
the life of the related patents or licenses, seven years for customer relationships and five years for assembled workforces. See Note
6 for more information on intangible assets.
Impairment
of Long-Lived Assets
Long-lived
assets, including certain identifiable intangibles held and to be used by the Company, are reviewed for impairment whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The Company continuously evaluates
the recoverability of its long-lived assets based on estimated future cash flows and the estimated liquidation value of such long-lived
assets and provides for impairment if such undiscounted cash flows are insufficient to recover the carrying amount of the long-lived
assets. If impairment exists, an adjustment is made to write the asset down to its fair value, and a loss is recorded as the difference
between the carrying value and fair value. Fair values are determined based on quoted market values, undiscounted cash flows or internal
and external appraisals, as applicable. Assets to be disposed of are carried at the lower of carrying value or estimated fair value less
cost to sell. No impairment was recorded during the nine months ended September 30, 2023 and 2022.
Investments
in Equity Securities
The
Company’s equity investments consist of nonmarketable equity securities in privately held companies without readily determinable
fair values. Unless accounted for under the equity method of accounting, the investments are reported at cost minus impairment, if any,
plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the
same issuer.
The
Company applies the equity method of accounting to investments when it has significant influence, but not controlling interest, in the
investee. Judgment regarding the level of influence over each equity method investment includes considering key factors such as ownership
interest, representation on the board of directors, participation in policy-making decisions and material intercompany transactions.
The Company’s proportionate share of the net income (loss) resulting from these investments is reported under the line item captioned
“Share of losses from equity method investment” in the Company’s Consolidated Statements of Operations. The Company’s
equity method investment is adjusted each period for the Company’s share of the investee’s income or loss and dividend paid,
if any. The Company classifies distributions received from its equity method investment using the cumulative earnings approach in the
Company’s Consolidated Statements of Cash Flows. As a result of the Precision Healing merger in April 2022 (see Note 3), the
Company did not have any investments which are recorded applying the equity method of accounting as of September 30, 2023.
The
Company has reviewed the carrying value of its investments and has determined there was no impairment or observable price changes as
of and for the nine months ended September 30, 2023 or 2022.
Fair
Value Measurement
As
defined in ASC Topic 820, Fair Value Measurement (“ASC 820”), fair value is the price that would be received to sell an asset
or paid to transfer a liability in an orderly transaction between market participants at the measurement date (exit price). The Company
utilizes market data or assumptions that market participants would use in pricing the asset or liability, including assumptions about
risk and the risks inherent in the inputs to the valuation technique. These inputs can be readily observable, market corroborated, or
generally unobservable. ASC 820 establishes a fair value hierarchy that prioritizes the inputs used to measure fair value. The hierarchy
gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurement) and
the lowest priority to unobservable inputs (Level 3 measurement). This fair value measurement framework applies at both initial and subsequent
measurement.
The
three levels of the fair value hierarchy defined by ASC 820 are as follows:
Level
1 – Quoted prices are available in active markets for identical assets or liabilities as of the reporting date. Active markets
are those in which transactions for the asset or liability occur in sufficient frequency and volume to provide pricing information on
an ongoing basis. Level 1 primarily consists of financial instruments such as exchange-traded derivatives, marketable securities and
listed equities.
Level
2 – Pricing inputs are other than quoted prices in active markets included in Level 1, which are either directly or indirectly
observable as of the reported date. Level 2 includes those financial instruments that are valued using models or other valuation methodologies.
These models are primarily industry-standard models that consider various assumptions, including quoted forward prices for commodities,
time value, volatility factors, and current market and contractual prices for the underlying instruments, as well as other relevant economic
measures. Substantially all these assumptions are observable in the marketplace throughout the full term of the instrument, can be derived
from observable data or are supported by observable levels at which transactions are executed in the marketplace. Instruments in this
category generally include nonexchange-traded derivatives such as commodity swaps, interest rate swaps, options and collars.
Level
3 – Pricing inputs include significant inputs that are generally less observable from objective sources. These inputs may be used
with internally developed methodologies that result in management’s best estimate of fair value.
The
carrying amounts of cash, accounts receivable, accounts payable and accrued expenses, other than acquisition-related accrued expenses,
approximate fair value because of the short-term nature of these instruments. The fair value of acquisition-related accrued expenses is categorized
as Level 2 of the fair value hierarchy. The value of these instruments has been estimated using discounted cash flow analysis based on
the Company’s incremental borrowing rate. The carrying value of the Company’s debt, which has
variable interest rates determined each month, approximates fair value based on instruments with similar terms (Level 2 inputs). The
fair value of the contingent earnout consideration and the acquisition date fair value of goodwill
and intangibles related to the acquisitions discussed in Notes 3, 4 and 5 are based on Level 3 inputs.
Liabilities
for contingent consideration are measured at fair value each reporting period, with the acquisition-date fair value included as part
of the consideration transferred. Subsequent changes in fair value are reported under the line item captioned “Change in fair value
of earnout liabilities” in the Company’s Consolidated Statements of Operations. The current year changes in fair value of earnout liabilities below are
as a result of a decrease in the estimated fair value of the earnout liabilities established at the time of the Company’s Precision Healing and
Scendia acquisitions. The following table sets forth a summary
of the changes in fair value for the Level 3 contingent earnout consideration.
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
Income
Taxes
Income
taxes are accounted for under the asset and liability method, whereby deferred income taxes are recorded for temporary differences between
financial statement carrying amounts and the tax basis of assets and liabilities. Deferred tax assets and liabilities reflect the tax
rates expected to be in effect for the years in which the differences are expected to reverse. A valuation allowance is provided if it
is more likely than not that some or all the deferred tax asset will not be realized.
Stock-based
Compensation
The
Company accounts for stock-based compensation to employees and nonemployees in accordance with Accounting Standards Update (“ASU”)
2018-07, Compensation – Stock Compensation (Topic 718). Stock-based compensation is measured at the grant date, based on the fair
value of the award, and is recognized as expense over the stipulated vesting period, if any. The Company estimates the fair value of
stock-based payments using the Black-Scholes option-pricing model for common stock options and warrants, and the closing price of the
Company’s common stock for grants of common stock, including restricted stock awards.
Research
and Development Costs
Research
and development (“R&D”) expenses consist of personnel-related expenses, including salaries and benefits for all personnel
directly engaged in R&D activities, contracted services, materials, prototype expenses and allocated overhead which is comprised
of lease expense and other facilities-related costs. R&D expenses include costs related to enhancements to the Company’s currently
available products and additional investments in the product, services and technologies development pipeline. The Company expenses R&D
costs as incurred.
Recently
Adopted Accounting Pronouncements
In
June 2016, the Financial Accounting Standards Board issued ASU 2016-13, Financial Instruments - Credit Losses (Topic 326). This update
amends the impairment model by requiring entities to use a forward-looking approach based on expected losses to estimate credit losses
for most financial assets and certain other instruments that are not measured at fair value through net income. The Company adopted the
new guidance effective January 1, 2023. The adoption did not have a material impact on the Company’s consolidated financial position,
results of operations or cash flows.
Recently
Issued Accounting Pronouncements
There
are no recently issued accounting pronouncements that have not yet been adopted that are expected to have a material effect on the Company’s
consolidated financial condition, results of operations or cash flows.
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v3.23.3
PRECISION HEALING MERGER
|
9 Months Ended |
Sep. 30, 2023 |
Precision Healing Merger |
|
PRECISION HEALING MERGER |
NOTE
3 – PRECISION HEALING MERGER
In
April 2022, the Company entered into a merger agreement by and among the Company, United Wound and Skin Solutions, LLC, a Delaware limited
liability company and wholly owned subsidiary of the Company, Precision Healing, PH Merger Sub I, Inc., a Delaware corporation, PH Merger
Sub II, LLC, a Delaware limited liability company, and Furneaux Capital Holdco, LLC (d/b/a BlueIO), solely in its capacity as the representative
of the securityholders of Precision Healing. On April 4, 2022 (the “Closing Date”), the merger parties closed the transactions
contemplated by the merger agreement and Precision Healing became a wholly owned subsidiary of the Company.
Precision
Healing is developing a diagnostic imager and lateral flow assay for assessing a patient’s wound and skin conditions. This comprehensive
skin and wound assessment technology is designed to quantify biochemical markers to determine the trajectory of a wound’s condition
to enable better diagnosis and treatment protocol. To date, Precision Healing has not generated revenues.
Pursuant
to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock, other than the Company, were entitled
to receive closing consideration, consisting of $125,966 in cash, which was paid to stockholders who were not accredited investors, 165,738
shares of the Company’s common stock, which was paid only to accredited investors, and the payment in cash of approximately $0.6
million of transaction expenses of Precision Healing. The Company recorded the issuance of the 165,738 shares to accredited investors
and cash payments to nonaccredited investors based on the closing price per share of the Company’s common stock on the Closing
Date, which was $30.75.
On
the Closing Date, the outstanding Precision Healing options previously granted under the Precision Healing Inc. 2020 Stock Option and
Grant Plan (the “Precision Healing Plan”) converted, pursuant to their terms, into options to acquire an aggregate of 144,191
shares of Company common stock with a weighted average exercise price of $10.71 per share. These options expire between August 2030 and
April 2031. In addition, outstanding and unexercised Precision Healing warrants converted into rights to receive warrants to purchase
(i) 4,424 shares of Company common stock with an initial exercise price of $7.32 per share and an expiration date of April 22, 2031,
and (ii) 12,301 shares of the Company’s common stock with an initial exercise price of $12.05 per share and an expiration date
of August 10, 2030.
Pursuant
to the merger agreement, the Company assumed sponsorship of the Precision Healing Plan, effective as of the Closing Date, as well as
the outstanding awards granted thereunder, the award agreements evidencing the grants of such awards and the remaining shares available
under the Precision Healing Plan, in each case adjusted in the manner set forth in the merger agreement. Concurrent with the assumption
of the Precision Healing Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC Topic 805, Business Combinations (“ASC 805”). The earnout consideration is payable in cash or, at the Company’s
election, is payable to accredited investors in shares of Company common stock at a price per share equal to the greater of (i) $27.13
or (ii) the average closing price of Company common stock for the 20 trading days prior to the date such earnout consideration is due
and payable. Pursuant to the merger agreement, a minimum percentage of the earnout consideration may be required to be issued to accredited
investors in shares of Company common stock for tax purposes. The amount and composition of the portion of earnout consideration payable
is subject to adjustment and offsets as set forth in the merger agreement.
As
the contingent earnout payments are not subject to any specific individual performance by the shareholders, the contingent shares are
not subject to ASC Topic 718, Compensation – Stock Compensation (“ASC 718”). Further, as the contingent consideration
was negotiated as part of the transfer of assets, the obligation was measured at fair value and included in the total purchase consideration
transferred. Additionally, the contingent earnout payments meet the criteria under ASC Topic 480, Distinguishing Liabilities from Equity
(“ASC 480”) as the monetary value of the shares to be issued is predominantly based on the exercise contingency (i.e., revenue
targets). Accordingly, the contingent consideration is classified as a liability at its estimated fair value at each reporting period
with the subsequent change in fair value recognized as a gain or loss in accordance with ASC 480.
The
total purchase consideration as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity
Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 165,738 | | |
$ | 5,096,444 | |
Fair value of assumed options | |
| 144,191 | | |
| 4,109,750 | |
Fair value of assumed warrants | |
| 16,725 | | |
| 502,895 | |
Cash paid to nonaccredited investors | |
| | | |
| 125,370 | |
Cash paid for fractional shares | |
| | | |
| 596 | |
Carrying value of equity method investment in Precision Healing | |
| | | |
| 1,803,440 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,882,151 | |
Direct transaction costs | |
| | | |
| 1,061,137 | |
Total purchase consideration | |
| | | |
$ | 16,581,783 | |
Based
on guidance provided by ASC 805, the Company recorded the Precision Healing merger as an asset acquisition due to the determination that
substantially all the fair value of the assets acquired was concentrated in a group of similar identifiable assets. The Company believes
the “substantially all” criterion was met with respect to the acquired intellectual property based on the Company’s
valuation models. These models assigned value to the acquired intellectual property based on estimated future cash flows. Accordingly,
the Company accounted for the merger as an asset acquisition.
The
purchase consideration, plus transaction costs, was allocated to the individual assets according to their fair values as a percentage
of the total fair value of the assets purchased, with no goodwill recognized. Based on the estimated fair value of the gross assets acquired,
the total fair value of the net assets acquired was primarily attributable to, and classified as, finite-lived intellectual property
and assembled workforce in the second quarter of 2022. The total purchase consideration was allocated based on the relative estimated
fair value of such assets as follows:
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 32,202 | |
Net working capital (excluding cash) | |
| (308,049 | ) |
Noncontrolling interest in Sanara Biologics, LLC | |
| | |
Customer relationships | |
| | |
Fixed assets, net | |
| 9,228 | |
Deferred tax assets | |
| 278,661 | |
Intellectual property | |
| 20,325,469 | |
Assembled workforce | |
| 664,839 | |
Deferred tax liabilities | |
| (4,420,567 | ) |
Goodwill | |
| | |
Net assets acquired | |
$ | 16,581,783 | |
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v3.23.3
SCENDIA PURCHASE AGREEMENT
|
9 Months Ended |
Sep. 30, 2023 |
Scendia Purchase Agreement |
|
SCENDIA PURCHASE AGREEMENT |
NOTE
4 – SCENDIA PURCHASE AGREEMENT
In
July 2022, the Company entered into a membership interest purchase agreement by and among the Company, Scendia, a Delaware limited liability
company, and Ryan Phillips (“Phillips”) pursuant to which, and in accordance with the terms and conditions set forth therein,
the Company acquired 100% of the issued and outstanding membership interests in Scendia from Phillips.
Scendia
provides clinicians and surgeons with a full line of regenerative and orthobiologic technologies for their patients through certain customer
accounts. Beginning in early 2022, the Company began co-promoting certain products with Scendia, including: (i) TEXAGEN Amniotic Membrane
Allograft, (ii) BiFORM Bioactive Moldable Matrix, (iii) ACTIGEN Verified Inductive Bone Matrix and (iv) ALLOCYTE Advanced Cellular Bone
Matrix. Prior to the acquisition, Scendia owned 50% of the issued and outstanding membership interests in Sanara Biologics, LLC (“Sanara
Biologics”), and the Company owned the remaining 50% of the membership interests. As a result of the acquisition, the Company indirectly
acquired all the interests in Sanara Biologics, such that the Company now holds 100% of the issued and outstanding equity interests in
Sanara Biologics.
Pursuant
to the purchase agreement, Phillips was entitled to receive closing consideration consisting of (i) approximately $1.6 million of cash,
subject to certain adjustments, and (ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing,
the Company withheld 94,798 shares of common stock with an agreed upon value of $1.95 million (the “Indemnity Holdback Shares”),
which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’ indemnification
obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023.
As
the contingent earnout payments are not subject to any specific individual performance by Phillips, the contingent shares are not subject
to ASC 718. Further, as the contingent consideration was negotiated as part of the transfer of assets, the obligation was measured at
fair value and included in the total purchase consideration transferred. Additionally, the contingent earnout payments meet the criteria
under ASC 480, as the monetary value of the shares to be issued is predominantly based on the exercise contingency (i.e., revenue targets).
Accordingly, the contingent consideration is classified as a liability at its estimated fair value at each reporting period with the
subsequent change in fair value recognized as a gain or loss in accordance with ASC 480.
The
total purchase consideration, subject to typical post-closing adjustments, as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 291,686 | | |
$ | 6,032,066 | |
Cash consideration | |
| | | |
| 1,562,668 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,000,000 | |
Total purchase consideration | |
| | | |
$ | 10,594,734 | |
Based
on guidance provided by ASC 805, the Company recorded the Scendia acquisition as a business combination. The purchase consideration was
allocated to the individual assets according to their fair values as a percentage of the total fair value of the net assets purchased.
The excess of the purchase consideration over the net assets purchased was recorded as goodwill. The total purchase consideration was
allocated as follows:
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 201,406 | |
Net working capital (excluding cash) | |
| 1,294,499 | |
Fixed assets, net | |
| 42,300 | |
Noncontrolling interest in Sanara Biologics, LLC | |
| 2,638 | |
Customer relationships | |
| 7,155,000 | |
Deferred tax liabilities | |
| (1,702,890 | ) |
Goodwill | |
| 3,601,781 | |
Net assets acquired | |
$ | 10,594,734 | |
The
goodwill acquired consists of expected synergies from the acquisition to the Company’s overall corporate strategy. The Company
does not expect any of the goodwill to be deductible for income tax purposes. The Company incurred acquisition costs of approximately
$187,000 in 2022, which is included in “Selling, general and administrative expenses” in the accompanying Consolidated Statements
of Operations.
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v3.23.3
APPLIED ASSET PURCHASE
|
9 Months Ended |
Sep. 30, 2023 |
Applied Asset Purchase |
|
APPLIED ASSET PURCHASE |
NOTE
5 – APPLIED ASSET PURCHASE
On
August 1, 2023, the Company entered into an Asset Purchase Agreement (the “Applied Purchase Agreement”) by and among the
Company, as guarantor, Sanara MedTech Applied Technologies, LLC, a Texas limited liability company and wholly owned subsidiary of
the Company (“SMAT”), The Hymed Group Corporation, a Delaware corporation (“Hymed”), Applied Nutritionals,
LLC, a Delaware limited liability company (“Applied”, and together with Hymed, the “Sellers”), and Dr.
George D. Petito (the “Owner”), pursuant to which SMAT acquired certain assets of the Sellers and the Owner, including,
among others, the Sellers’ and Owner’s inventory, intellectual property, manufacturing and related equipment, goodwill,
rights and claims, other than certain excluded assets, all as more specifically set forth in the Applied Purchase Agreement
(collectively, the “Applied Purchased Assets”), and assumed certain Assumed Liabilities (as defined in the Applied
Purchase Agreement), upon the terms and subject to the conditions set forth in the Applied Purchase Agreement (such transaction, the
“Applied Asset Purchase”). The Applied Purchased Assets include the underlying intellectual property of, as well as the
rights to manufacture and sell, CellerateRX Surgical Activated Collagen (Powder and Gel) (“CellerateRX Surgical”) and
HYCOL Hydrolyzed Collagen (Powder and Gel) (“HYCOL”) products for human wound care use.
The
Applied Purchased Assets were purchased for an initial aggregate purchase price of $15.25 million, consisting of (i) $9.75 million in
cash (the “Cash Closing Consideration”), (ii) 73,809 shares of the Company’s common stock (the “Stock Closing
Consideration”) with an agreed upon value of $3.0 million and (iii) $2.5 million in cash (the “Installment Payments”),
to be paid in four equal installments on each of the next four anniversaries of the closing of the Applied Asset Purchase (the “Closing”).
Prior
to the Closing, the Company licensed certain of its products from Applied through a sublicense agreement (the “Sublicense Agreement”)
with CGI Cellerate RX, LLC (“CGI Cellerate RX”), a related party (see Note 13 for additional information regarding transactions with related parties). Pursuant
to the Sublicense Agreement, the Company has an exclusive, world-wide sublicense to distribute CellerateRX Surgical and HYCOL products
into the surgical and wound care markets. In connection with the Applied Asset Purchase, Applied assigned its license agreement with
CGI Cellerate RX to SMAT. Since the Closing of the Applied Asset Purchase, Sanara indirectly makes intercompany royalty payments to SMAT
at the same rate as set forth in the Sublicense Agreement. Effective August 1, 2023, these intercompany royalty payments and the offsetting cost of goods sold are eliminated
on a consolidated basis.
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive up to an additional $10.0 million (the “Applied Earnout”), which is payable to the
Sellers in cash, upon the achievement of certain performance thresholds relating to SMAT’s collections from net sales of a collagen-based
product currently under development. Upon expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned
the entirety of the Applied Earnout, SMAT shall pay the Sellers a pro-rata amount of the Applied Earnout based on collections from net
sales of the product, with such amount to be due credited against any Applied Earnout payments already made by SMAT (the “True-Up
Payment”). The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already made by SMAT, may be earned
at any point in the future, including after the True-Up Payment is made.
In
connection with the Applied Asset Purchase and pursuant to the Applied Purchase Agreement, effective August 1, 2023, the Company entered
into a professional services agreement (the “Petito Services Agreement”) with the Owner, pursuant to which the Owner, as
an independent contractor, agreed to provide certain services to the Company, including, among other things, assisting with the development
of products already in development and assisting with research, development, formulation, invention and manufacturing of any future products
(the “Petito Services”). As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of
$12,000 per month during the term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual
collections from net sales of certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment
equal to five percent (5%) for the first $50.0 million in aggregate collections from net sales of certain future products and a royalty
payment of two and one-half percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding
$50.0 million but up to $100.0 million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted
by the Company and (v) $1.0 million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect
to the incentive payments described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
The
Petito Services Agreement has an initial term of three years and is subject to automatic successive one-month renewals unless earlier
terminated in accordance with its terms. The Petito Services Agreement may be terminated upon the Owner’s death or disability or
by the Company or the Owner “For Cause” (as defined in the Petito Services Agreement); provided, however, that the base salary
described in (i) of the foregoing paragraph shall survive termination through the three-year initial term and the royalty payments and
incentive payments described in (ii)-(v) of the foregoing paragraph shall survive termination of the Petito Services Agreement.
As
the contingent consideration was negotiated as part of the transfer of assets, the contingent obligations were
measured at fair value and included in the total purchase consideration transferred. Accordingly, the contingent consideration
is classified as a liability at its estimated fair value at each reporting period with the subsequent change in fair value recognized
as a gain or loss.
The
total purchase consideration for the Applied Asset Purchase as determined by the Company was as follows:
SCHEDULE
OF PURCHASE CONSIDERATION
Consideration | |
Equity Shares | | |
Dollar Value | |
Cash Closing Consideration | |
| | | |
$ | 9,750,000 | |
Fair value of Stock Closing Consideration | |
| 73,809 | | |
| 3,089,645 | |
Fair value of Installment Payments | |
| | | |
| 2,040,808 | |
Cash paid for inventory | |
| | | |
| 30,007 | |
Fair value of Petito Services Agreement defined payments | |
| | | |
| 825,834 | |
Fair value of Petito Services Agreement contingent consideration | |
| | | |
| 893,000 | |
Direct transaction costs | |
| | | |
| 162,743 | |
Total purchase consideration | |
| | | |
$ | 16,792,037 | |
Based
on guidance provided by ASC 805, the Company recorded the Applied Asset Purchase as an asset acquisition due to the determination that
substantially all the fair value of the assets acquired was concentrated in a group of similar identifiable assets. The Company believes
the “substantially all” criterion was met with respect to the acquired intellectual property being the only significant asset
acquired. Accordingly, the Company accounted for the transaction as an asset acquisition.
The
purchase consideration, plus transaction costs, was allocated to the individual assets according to their fair values as a percentage
of the total fair value of the assets purchased, with no goodwill recognized. Based on the estimated fair value of the gross assets acquired,
the total fair value of the net assets acquired was primarily attributable to, and classified as, finite-lived intellectual property
in the third quarter of 2023. The total purchase consideration was allocated based on the relative estimated fair value of such assets
as follows:
SCHEDULE
OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Inventory | |
$ | 30,007 | |
Equipment | |
| 33,062 | |
Intellectual property | |
| 16,728,968 | |
Net assets acquired | |
$ | 16,792,037 | |
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v3.23.3
INTANGIBLE ASSETS
|
9 Months Ended |
Sep. 30, 2023 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
INTANGIBLE ASSETS |
NOTE
6 – INTANGIBLE ASSETS
The
carrying values of the Company’s intangible assets were as follows for the periods presented:
SCHEDULE OF FINITE LIVED INTANGIBLE ASSETS
| |
September 30, 2023 | | |
December 31, 2022 | |
| |
| | |
Accumulated | | |
| | |
| | |
Accumulated | | |
| |
| |
Cost | | |
Amortization | | |
Net | | |
Cost | | |
Amortization | | |
Net | |
Amortizable Intangible Assets: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Product licenses | |
$ | 4,793,879 | | |
$ | (1,246,115 | ) | |
$ | 3,547,764 | | |
$ | 4,793,879 | | |
$ | (980,583 | ) | |
$ | 3,813,296 | |
Patents and other IP | |
| 38,664,548 | | |
| (2,598,220 | ) | |
| 36,066,328 | | |
| 21,935,580 | | |
| (1,492,057 | ) | |
| 20,443,523 | |
Customer relationships and other | |
| 7,947,332 | | |
| (1,569,958 | ) | |
| 6,377,374 | | |
| 7,947,332 | | |
| (694,171 | ) | |
| 7,253,161 | |
Total | |
$ | 51,405,759 | | |
$ | (5,414,293 | ) | |
$ | 45,991,466 | | |
$ | 34,676,791 | | |
$ | (3,166,811 | ) | |
$ | 31,509,980 | |
As
of September 30, 2023, the weighted-average amortization period for finite-lived intangible assets was 14.5 years. Amortization expense
related to intangible assets was $881,079 and $708,534 for the three months ended September 30, 2023 and 2022, respectively, and $2,247,482
and $1,256,097 for the nine months ended September 30, 2023 and 2022, respectively. The estimated remaining amortization expense as of
September 30, 2023 for finite-lived intangible assets is as follows:
SCHEDULE OF FUTURE AMORTIZATION EXPENSE
| |
| | |
Remainder of 2023 | |
$ | 974,018 | |
2024 | |
| 3,896,070 | |
2025 | |
| 3,896,070 | |
2026 | |
| 3,878,815 | |
2027 | |
| 3,764,962 | |
2028 | |
| 3,731,721 | |
Thereafter | |
| 25,849,810 | |
Total | |
$ | 45,991,466 | |
The
Company has reviewed the carrying value of intangible assets and has determined there was no impairment during either of the nine months
ended September 30, 2023 or 2022.
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v3.23.3
INVESTMENTS IN EQUITY SECURITIES
|
9 Months Ended |
Sep. 30, 2023 |
Schedule of Investments [Abstract] |
|
INVESTMENTS IN EQUITY SECURITIES |
NOTE
7 – INVESTMENTS IN EQUITY SECURITIES
The
Company’s equity investments consist of nonmarketable equity securities in privately held companies without readily determinable
fair values. Unless accounted for under the equity method of accounting, the investments are reported at cost minus impairment, if any,
plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the
same issuer.
In
July 2020, the Company made a $500,000 long-term investment to purchase certain nonmarketable securities consisting of 7,142,857 Series
B-2 Preferred Shares of Direct Dermatology Inc. (“DirectDerm”), representing approximately 2.9% ownership of DirectDerm at
that time. Through this investment, the Company received exclusive rights to utilize DirectDerm’s technology in all acute and post-acute
care settings such as skilled nursing facilities, home health and wound clinics. The Company does not have the ability to exercise significant
influence over DirectDerm’s operating and financial activities. In 2021, the Company purchased an additional 3,571,430 shares of
DirectDerm’s Series B-2 Preferred for $250,000. In March 2022, the Company purchased an additional 3,571,429 shares of DirectDerm’s
Series B-2 Preferred for $250,000. The Company’s ownership of DirectDerm was approximately 8.1% as of September 30, 2023.
In
November 2020, the Company entered into agreements to purchase certain nonmarketable securities consisting of 150,000 shares of Series
A Convertible Preferred Stock (the “Series A Stock”) of Precision Healing for an aggregate purchase price of $600,000. The
Series A Stock was convertible into 150,000 shares of common stock of Precision Healing and had a senior liquidation preference relative
to the common shareholders. This initial investment represented approximately 12.6% ownership of Precision Healing’s outstanding
voting securities. In February 2021, the Company invested $600,000 to purchase 150,000 additional shares of Series A Stock which was
convertible into 150,000 shares of common stock of Precision Healing. This resulted in ownership of approximately 22.4% of Precision
Healing’s outstanding voting securities. With this level of significant influence, the Company transitioned to the equity method
of accounting for this investment. In June 2021, the Company invested $500,000 for 125,000 additional shares of Series A Stock, which
increased the Company’s ownership of Precision Healing’s outstanding voting securities to approximately 29.0%. In October
and December of 2021, 125,000 and 150,000 more shares of Series A Stock were purchased for $500,000 and $600,000, respectively.
As
discussed above, in April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became
a wholly owned subsidiary of the Company (see Note 3 for more information). As a result of the merger, the Company’s equity method
investment in Precision Healing ceased in April 2022. The Company recorded $379,633 in the nine months ended September 30, 2022 as its
share of the loss from this equity method investment for the period prior to acquisition.
In
June 2021, the Company invested $2,084,278 to purchase 278,587 Class A Preferred Shares (the “Pixalere Shares”) of Canada-based
Pixalere Healthcare Inc. (“Pixalere”). The Pixalere Shares are convertible into approximately 27.3% of the outstanding equity
of Pixalere. Pixalere provides a cloud-based wound care software tool that empowers nurses, specialists and administrators to deliver
better care for patients. In connection with the Company’s purchase of the Pixalere Shares, Pixalere granted Pixalere Healthcare
USA, LLC (“Pixalere USA”), a subsidiary of the Company, a royalty-free exclusive license to use the Pixalere software and
platform in the United States. In conjunction with the grant of the license, the Company issued Pixalere a 27.3% equity ownership interest
in Pixalere USA valued at $93,879.
The
Company has reviewed the characteristics of the Pixalere Shares in accordance with ASC Topic 323, Investments – Equity Method and
Joint Ventures. Due to the substantive liquidation preferences of the Pixalere Shares over Pixalere’s common stock, the Pixalere
Shares are not “in-substance” common stock, and therefore, the Company does not utilize the equity method of accounting for
this investment. In accordance with ASC Topic 321, Investments - Equity Securities, this investment was reported at cost as of September
30, 2023.
The
following summarizes the Company’s investments for the periods presented:
SCHEDULE
OF INVESTMENTS
| |
September
30, 2023 | | |
December
31, 2022 | |
| |
| Carrying
Amount | | |
| Economic
Interest | | |
| Carrying
Amount | | |
| Economic
Interest | |
Equity
Method Investment | |
| | | |
| | | |
| | | |
| | |
Precision
Healing Inc. | |
$ | - | | |
| - | % | |
$ | - | | |
| - | % |
| |
| | | |
| | | |
| | | |
| | |
Cost
Method Investments | |
| | | |
| | | |
| | | |
| | |
Direct
Dermatology, Inc. | |
| 1,000,000 | | |
| | | |
| 1,000,000 | | |
| | |
Pixalere
Healthcare Inc. | |
| 2,084,278 | | |
| | | |
| 2,084,278 | | |
| | |
Total
Cost Method Investments | |
| 3,084,278 | | |
| | | |
| 3,084,278 | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Total
Investments | |
$ | 3,084,278 | | |
| | | |
$ | 3,084,278 | | |
| | |
The
following summarizes the loss from the equity method investment reflected in the Consolidated Statements of Operations:
SCHEDULE OF LOSS FROM EQUITY METHOD INVESTMENT
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three
Months ended September 30, | | |
Nine
Months Ended September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Investment | |
| | |
| | |
| | |
| |
Precision
Healing Inc. | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
| |
| | | |
| | | |
| | | |
| | |
Total | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
Loss from equity method
investment | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
|
X |
- DefinitionThe entire disclosure for investment holdings. This includes the long positions of investments for the entity. It contains investments in affiliated and unaffiliated issuers. The investments include securities and non securities (i.e. commodities and futures contracts).
+ ReferencesReference 1: http://www.xbrl.org/2003/role/disclosureRef -Topic 946 -SubTopic 210 -Name Accounting Standards Codification -Section 50 -Paragraph 12 -Publisher FASB -URI https://asc.fasb.org//1943274/2147480524/946-210-50-12
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v3.23.3
OPERATING LEASES
|
9 Months Ended |
Sep. 30, 2023 |
Operating Leases |
|
OPERATING LEASES |
NOTE
8 – OPERATING LEASES
The
Company periodically enters operating lease contracts for office space and equipment. Arrangements are evaluated at inception to determine
whether such arrangements constitute a lease. Right of use assets (“ROU assets”) represent the right to use an underlying
asset for the lease term and lease liabilities represent the obligation to make lease payments arising from the lease. Operating lease
ROU assets and liabilities were recognized on the transition date based on the present value of lease payments over the respective lease
term, with the office space ROU asset adjusted for deferred rent liability.
The
Company has three material operating leases for office space. In March and September 2023, the Company amended its primary office lease
to obtain additional space, as well as extend the term. The leases have remaining lease terms of 87, 40 and 23 months as of September
30, 2023. For practical expediency, the Company has elected to not recognize ROU assets and lease liabilities related to short-term leases.
In
accordance with ASC Topic 842, Leases, the Company has recorded ROU assets of $2,094,188 and a related lease liability of $2,168,499
as of September 30, 2023. The Company recorded lease expense of $295,268 and $210,317 for the nine months ended September 30, 2023 and
2022, respectively, for its leased assets. Cash paid for amounts included in the measurement of operating lease liabilities was $264,291
and $210,897 for the nine months ended September 30, 2023 and 2022, respectively. The present value of the Company’s operating
lease liabilities as of September 30, 2023 is shown below.
Maturity
of Operating Lease Liabilities
SCHEDULE OF OPERATING LEASE LIABILITY
| |
September 30,
2023 | |
Remainder of 2023 | |
$ | 116,285 | |
2024 | |
| 505,017 | |
2025 | |
| 532,053 | |
2026 | |
| 379,529 | |
2027 | |
| 297,947 | |
2028 | |
| 295,689 | |
Thereafter | |
| 604,049 | |
Total lease payments | |
| 2,730,569 | |
Less imputed interest | |
| (562,070 | ) |
Present Value of Lease Liabilities | |
$ | 2,168,499 | |
| |
| | |
Operating lease liabilities – current | |
| 322,206 | |
Operating lease liabilities – long-term | |
| 1,846,293 | |
As
of September 30, 2023, the Company’s operating leases had a weighted average remaining lease term of 6.0 years and a weighted average
discount rate of 7.59%.
|
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- DefinitionThe entire disclosure for operating leases of lessee. Includes, but is not limited to, description of operating lease and maturity analysis of operating lease liability.
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v3.23.3
DEBT AND CREDIT FACILITIES
|
9 Months Ended |
Sep. 30, 2023 |
Debt And Credit Facilities |
|
DEBT AND CREDIT FACILITIES |
NOTE
9 – DEBT AND CREDIT FACILITIES
In
connection with the entry into the Applied Purchase Agreement, on August 1, 2023, SMAT, as borrower, and the Company, as guarantor, entered
into a loan agreement (the “Loan Agreement”) with Cadence Bank (the “Bank”) providing for, among other things,
an advancing term loan in the aggregate principal amount of $12.0 million (the “Term Loan”), which was evidenced by an advancing
promissory note. Pursuant to the Loan Agreement, the Bank agreed to make, at any time and from time to time prior to February 1, 2024,
one or more advances to SMAT.
The
proceeds of the advances under the Loan Agreement will be used for working capital and for purposes of financing up to one hundred percent
(100%) of the Cash Closing Consideration and Installment Payments for the Applied Asset Purchase and related fees and expenses, including
any subsequent payments that may be due to the Sellers after the Closing. On August 1, 2023, the Bank, at the request of SMAT, made an
advance for $9.75 million. The proceeds from the advance were used to fund the Cash Closing Consideration for the Applied Asset Purchase.
Advances
under the Term Loan will begin amortizing in monthly installments commencing on August 5, 2024. All remaining unpaid balances under the
Term Loan are due and payable in full on August 1, 2028 (the “Maturity Date”). SMAT may prepay amounts due under the Term
Loan. All accrued but unpaid interest on the unpaid principal balance of outstanding advances is due and payable monthly, beginning on
September 5, 2023 and continuing monthly on the fifth day of each month thereafter until the Maturity Date. The unpaid principal balance
of outstanding advances bears interest, subject to certain conditions, at the lesser of the Maximum Rate (as defined in the Loan Agreement)
or the Base Rate, which is for any day, a rate per annum equal to the term secured overnight financing rate (Term SOFR) (as administered
by the Federal Reserve Bank of New York) for a one-month tenor in effect on such day plus three percent (3.0%).
The
obligations of SMAT under the Loan Agreement and the other loan documents delivered in connection therewith are guaranteed by the Company
and are secured by a first priority security interest in substantially all of the existing and future assets of SMAT.
The
Loan Agreement contains customary representations and warranties and certain covenants that limit (subject to certain exceptions) the
ability of SMAT and the Company to, among other things, (i) create, assume or guarantee certain liabilities, (ii) create, assume or suffer
liens securing indebtedness, (iii) make or permit loans and advances, (iv) acquire any assets outside the ordinary course of business,
(v) consolidate, merge or sell all or a material part of its assets, (vi) pay dividends or other distributions on, or redeem or repurchase,
interest in an obligor, including the Company, as guarantor (vii) cease, suspend or materially curtail business operations or (viii)
engage in certain affiliate transactions. In addition, the Loan Agreement contains financial covenants that require SMAT to maintain
(i) a minimum Debt Services Coverage Ratio of 1.2 to 1.0 as of the last day of each applicable fiscal quarter and (ii) a maximum Cash
Flow Leverage Ratio of not more than (a) 4.5 to 1.0 as of the last day of the fiscal quarter ending on September 30, 2023, (b) 4.0 to
1.0 as of the last day of each fiscal quarter ending on December 31, 2023 and March 31, 2024, (c) 3.5 to 1.0 as of the last day of each
fiscal quarter ending June 30, 2024 and September 30, 2024 and (d) 3.0 to 1.0 as of the last day of each fiscal quarter thereafter. Pursuant
to the Loan Agreement, in the event that SMAT fails to comply with the financial covenants described above, the Company is required to
contribute cash to SMAT in an amount equal to the amount required to satisfy the financial covenants. During the three months ended September 30, 2023, the Company contributed an immaterial amount of cash to SMAT in order to permit SMAT
to be in compliance with the financial covenants under the Loan Agreement. The Company was in compliance with
the financial covenants under the Loan Agreement as of September 30, 2023.
The
Loan Agreement also contains customary events of default. If such an event of default occurs, the Bank would be entitled to take various
actions, including the acceleration of amounts due under the Loan Agreement and actions permitted to be taken by a secured creditor.
The
table below presents the components of outstanding debt for the periods presented:
SCHEDULE
OF LONG-TERM DEBT
| |
September 30, 2023 | | |
December 31, 2022 | |
Term Loan | |
$ | 9,750,000 | | |
$ | - | |
Total debt | |
| 9,750,000 | | |
| - | |
Less: debt issuance costs, net of accumulated amortization of $2,055 and zero | |
| (59,603 | ) | |
| - | |
Long-term debt | |
| 9,690,397 | | |
| - | |
Less: current portion of debt | |
| 232,143 | | |
| - | |
Long-term debt, net of current portion | |
$ | 9,458,254 | | |
$ | - | |
As
of September 30, 2023, the interest rate on the advance under the Term Loan was 8.3%.
The
table below presents the aggregate maturities of the Company’s outstanding debt as of September 30, 2023:
SCHEDULE
OF MATURITIES OUTSTANDING DEBT
Year | |
Total | |
Remainder of 2023 | |
$ | - | |
2024 | |
| 580,357 | |
2025 | |
| 1,625,000 | |
2026 | |
| 1,950,000 | |
2027 | |
| 1,950,000 | |
2028 | |
| 3,644,643 | |
Thereafter | |
| - | |
Total debt | |
$ | 9,750,000 | |
In
connection with the Term Loan, the Company incurred $61,658
in debt issuance costs during the three months ended September 30, 2023. Debt issuance costs are amortized to “Interest
expense and other” on the Consolidated Statement of Operations over the life of the debt to which they pertain. The total
unamortized debt issuance costs were $59,603
and zero
as of September 30, 2023 and December 31, 2022, respectively. Debt issuance costs are included in “Long-term debt, net of
current portion” on the Consolidated Balance Sheets. Amortization expense related to debt issuance costs was $2,055
and zero
for the three and nine months ended September 30, 2023 and 2022, respectively.
|
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v3.23.3
COMMITMENTS AND CONTINGENCIES
|
9 Months Ended |
Sep. 30, 2023 |
Commitments and Contingencies Disclosure [Abstract] |
|
COMMITMENTS AND CONTINGENCIES |
NOTE
10 – COMMITMENTS AND CONTINGENCIES
License
Agreements and Royalties
CellerateRX
Surgical Activated Collagen
In
August 2018, the Company entered into the Sublicense Agreement with CGI Cellerate RX to distribute CellerateRX Surgical and HYCOL
products into the surgical and wound care markets. Pursuant to the Sublicense Agreement, the Company pays royalties of 3-5% of
annual collected net sales of CellerateRX Surgical and HYCOL. As amended in January 2021, the term of the sublicense extends through
May 2050, with automatic successive year-to-year renewal terms thereafter so long as the Company’s Net Sales (as defined in
the Sublicense Agreement) each year are equal to or in excess of $1,000,000. If the Company’s Net Sales fall below $1,000,000
for any year after the initial expiration date, CGI Cellerate RX will have the right to terminate the Sublicense Agreement upon
written notice.
Under
this agreement, royalty expense, which is recorded in “Cost of goods sold” in the accompanying Consolidated Statements
of Operations, totaled a benefit of $9,209 for
the three months ended September 30, 2023 due to the reversal of an accrual and $432,809
of expense for the three months ended September 30, 2022, respectively. Royalty expense totaled $1,060,035 and
$1,245,775 for
the nine months ended September 30, 2023 and 2022, respectively. Sales of CellerateRX Surgical comprised the substantial majority of
the Company’s sales during the three and nine months ended September 30, 2023 and 2022.
As
discussed further in Note 5, on August 1, 2023, the Company purchased certain assets from Applied, including the underlying
intellectual property of, as well as the rights to manufacture and sell, CellerateRX Surgical and HYCOL products. In connection with
the Applied Asset Purchase, Applied assigned its license agreement with CGI Cellerate RX to SMAT. Since the Closing, Sanara
indirectly makes intercompany royalty payments to SMAT at the same rate as set forth in the Sublicense Agreement. Effective August 1, 2023, these intercompany royalty payments and the offsetting cost of goods sold are eliminated
on a consolidated basis.
BIAKŌS
Antimicrobial Wound Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser
In
July 2019, the Company executed a license agreement with Rochal Industries, LLC (“Rochal”), a related party, pursuant to
which the Company acquired an exclusive world-wide license to market, sell and further develop antimicrobial products for the prevention
and treatment of microbes on the human body utilizing certain Rochal patents and pending patent applications (the “BIAKŌS
License Agreement”). Currently, the products covered by the BIAKŌS License Agreement are BIAKŌS Antimicrobial Wound
Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser. Both products are 510(k) cleared.
Future
commitments under the terms of the BIAKŌS License Agreement include:
| ● | The
Company pays Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to Rochal
was $120,000 for 2022 and will increase by $10,000 each subsequent calendar year up to a
maximum amount of $150,000. |
| ● | The
Company pays additional royalty annually based on specific net profit targets from sales
of the licensed products, subject to a maximum of $1,000,000 during any calendar year. |
Unless
previously terminated by the parties, the BIAKŌS License Agreement expires with the related patents in December 2031.
Under
this agreement, royalty expense, which is recorded in “Cost of goods sold” in the accompanying Consolidated Statements of
Operations, was $32,499 and $30,000 for the three months ended September 30, 2023 and 2022, respectively. For the nine months ended September
30, 2023 and 2022, royalty expense was $97,499 and $90,000, respectively. The Company’s Executive Chairman is a director of Rochal,
and indirectly a significant shareholder of Rochal, and through the potential exercise of warrants, a majority shareholder of Rochal.
Another one of the Company’s directors is also a director and significant shareholder of Rochal.
CuraShield
Antimicrobial Barrier Film and No Sting Skin Protectant
In
October 2019, the Company executed a license agreement with Rochal pursuant to which the Company acquired an exclusive world-wide license
to market, sell and further develop certain antimicrobial barrier film and skin protectant products for use in the human health care
market utilizing certain Rochal patents and pending patent applications (the “ABF License Agreement”). Currently, the products
covered by the ABF License Agreement are CuraShield Antimicrobial Barrier Film and a no sting skin protectant product.
Future
commitments under the terms of the ABF License Agreement include:
| ● | The
Company will pay Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to
Rochal will be $50,000 beginning with the first full calendar year following the year in
which first commercial sales of the products occur. The annual minimum royalty will increase
by 10% each subsequent calendar year up to a maximum amount of $75,000. |
| ● | The
Company will pay additional royalties annually based on specific net profit targets from
sales of the licensed products, subject to a maximum of $500,000 during any calendar year. |
Unless
previously terminated or extended by the parties, the ABF License Agreement will terminate upon expiration of the last U.S. patent in
October 2033. No commercial sales or royalties had been recognized under this agreement as of September 30, 2023.
Debrider
License Agreement
In
May 2020, the Company executed a product license agreement with Rochal, pursuant to which the Company acquired an exclusive world-wide
license to market, sell and further develop a debrider for human medical use to enhance skin condition or treat or relieve skin disorders,
excluding uses primarily for beauty, cosmetic, or toiletry purposes (the “Debrider License Agreement”).
Future
commitments under the terms of the Debrider License Agreement include:
| ● | Upon
FDA clearance of the licensed products, the Company will pay Rochal $500,000 in cash and
an additional $1,000,000, which at the Company’s option may be paid in any combination
of cash and its common stock. |
| ● | The
Company will pay Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to
Rochal will be $100,000 beginning with the first full calendar year following the year in
which first commercial sales of the licensed products occur and increase by 10% each subsequent
calendar year up to a maximum amount of $150,000. |
| ● | The
Company will pay additional royalty annually based on specific net profit targets from sales
of the licensed products, subject to a maximum of $1,000,000 during any calendar year. |
Unless
previously terminated or extended by the parties, the Debrider License Agreement will expire in October 2034. No commercial sales or
royalties have been recognized under this agreement as of September 30, 2023.
Resorbable
Bone Hemostat
The
Company acquired a patent in 2009 for a resorbable bone hemostat and delivery system for orthopedic bone void fillers. In connection
with the patent acquisition, the Company entered into a royalty agreement to pay 8% of the Company’s net revenues, including royalty
revenues, generated from products that utilize the Company’s acquired patented bone hemostat and delivery system. This patent is
not part of the Company’s long-term strategic focus. The Company subsequently licensed the patent to a third party to market a
bone void filler product for which the Company receives a 2% royalty on product sales through the end of 2023, with annual minimum royalties
of $201,000. To date, royalty revenues received by the Company related to this licensing agreement have not exceeded the annual minimum
of $201,000 ($50,250 per quarter). Therefore, the Company’s annual royalty obligation has been $16,080 ($4,020 per quarter), with
the expense being reported in “Cost of goods sold” in the accompanying Consolidated Statements of Operations.
Rochal
Asset Acquisition
In
July 2021, the Company entered into an asset purchase agreement with Rochal effective July 1, 2021, pursuant to which the Company purchased
certain assets of Rochal. Pursuant to the asset purchase agreement, for the three-year period after the effective date, Rochal is entitled
to receive consideration for any new product relating to the business that is directly and primarily based on an invention conceived
and reduced to practice by a member or members of Rochal’s science team. For the three-year period after the effective date, Rochal
is also entitled to receive an amount in cash equal to twenty-five percent of the proceeds received for any Grant (as defined in the
asset purchase agreement) by either the Company or Rochal. In addition, the Company agreed to use commercially reasonable efforts to
perform Minimum Development Efforts (as defined in the asset purchase agreement) with respect to certain products under development,
which if obtained, will entitle the Company to intellectual property rights from Rochal in respect of such products.
Precision
Healing Merger Agreement
In
April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became a wholly owned
subsidiary of the Company. Pursuant to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock,
other than the Company, were entitled to receive closing consideration, consisting of $125,966 in cash consideration, which was paid
to stockholders who were not accredited investors, 165,738 shares of the Company’s common stock, which was paid only to accredited
investors, and the payment in cash of approximately $0.6 million of transaction expenses of Precision Healing. The Company recorded the
issuance of the 165,738 shares to accredited investors and cash payments to nonaccredited investors based on the closing price per share
of the Company’s common stock on April 4, 2022, which was $30.75.
Upon
the closing of the merger, the Precision Healing outstanding options previously granted under the Precision Healing Plan converted, pursuant
to their terms, into options to acquire an aggregate of 144,191 shares of Company common stock with a weighted average exercise price
of $10.71 per share. These options expire between August 2030 and April 2031. In addition, outstanding and unexercised Precision Healing
warrants converted into rights to receive warrants to purchase (i) 4,424 shares of Company common stock with an initial exercise price
of $7.32 per share and an expiration date of April 22, 2031, and (ii) 12,301 shares of the Company’s common stock with an initial
exercise price of $12.05 per share and an expiration date of August 10, 2030. Concurrent with the assumption of the Precision Healing
Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC 805. The earnout consideration is payable in cash or, at the Company’s election, is payable to accredited investors
in shares of Company common stock at a price per share equal to the greater of (i) $27.13 or (ii) the average closing price of Company
common stock for the 20 trading days prior to the date such earnout consideration is due and payable. Pursuant to the merger agreement,
a minimum percentage of the earnout consideration may be required to be issued to accredited investors in shares of Company common stock
for tax purposes. The amount and composition of the portion of earnout consideration payable is subject to adjustment and offsets as
set forth in the merger agreement. See Note 3 for more information regarding the merger with Precision Healing.
Scendia
Purchase Agreement
In
July 2022, the Company closed the Scendia acquisition pursuant to which Scendia became a wholly owned subsidiary of the Company. Pursuant
to the purchase agreement, the aggregate consideration for the acquisition at closing was approximately $7.6 million, subject to customary
post-closing adjustments. The consideration consisted of (i) approximately $1.6 million of cash, subject to certain adjustments, and
(ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing, the Company withheld 94,798 Indemnity
Holdback Shares, which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’
indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023. The Company expects the second earnout payment to be made in the third quarter of 2024.
See Note 4 for more information regarding the acquisition of Scendia.
Applied
Asset Purchase
On
August 1, 2023, the Company closed the Applied Asset Purchase. The Applied Purchased Assets were purchased for an initial aggregate
purchase price of $15.25
million, consisting of (i) the Cash Closing Consideration , (ii) the Stock Closing Consideration and (iii) the Installment
Payments.
In
addition to the Cash Closing Consideration, Stock Closing Consideration and Installment Payments, the Applied Purchase Agreement provides
that the Sellers are entitled to receive the Applied Earnout, which is payable to the Sellers in cash, upon the achievement of certain
performance thresholds relating to SMAT’s collections from net sales of a collagen-based product currently under development. Upon
expiration of the seventh anniversary of the Closing, to the extent the Sellers have not earned the entirety of the Applied Earnout,
SMAT shall pay the Sellers the True-Up Payment. The Applied Earnout, minus the True-Up Payment and any Applied Earnout payments already
made by SMAT, may be earned at any point in the future, including after the True-Up Payment is made.
In
connection with the Applied Asset Purchase and pursuant to the Applied Purchase Agreement, effective August 1, 2023, the Company entered
into the Petito Services Agreement with the Owner, pursuant to which the Owner, as an independent contractor, agreed to provide the Petito
Services. As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of $12,000 per month during the
term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual collections from net sales of
certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment equal to five percent (5%) for
the first $50.0 million in aggregate collections from net sales of certain future products and a royalty payment of two and one-half
percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding $50.0 million but up to $100.0
million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted by the Company and (v) $1.0
million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect to the incentive payments
described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
The
Petito Services Agreement has an initial term of three years and is subject to automatic successive one-month renewals unless earlier
terminated in accordance with its terms. The Petito Services Agreement may be terminated upon the Owner’s death or disability or
by the Company or the Owner “For Cause” (as defined in the Petito Services Agreement); provided, however, that the base salary
described in (i) of the foregoing paragraph shall survive termination through the three-year initial term and the royalty payments and
incentive payments described in (ii)-(v) of the foregoing paragraph shall survive termination of the Petito Services Agreement.
Other
Commitments
In
May 2019, the Company organized Sanara Pulsar, LLC (“Sanara Pulsar”), a Texas limited liability company, which was owned
60% by the Company’s wholly owned subsidiary Cellerate, LLC, and 40% owned by Wound Care Solutions, Limited (“WCS”),
an unaffiliated company registered in the United Kingdom. At the time of the formation of Sanara Pulsar, it and WCS, entered into a supply
agreement whereby Sanara Pulsar became the exclusive distributor in the United States of certain wound care products that utilize intellectual
property developed and owned by WCS. Pursuant to the operating agreement of Sanara Pulsar, in the event WCS’s annual Form K-l does
not allocate to WCS net income of at least $200,000 (the “Target Net Income”), the Company is required, within 30 days after
such determination, to pay WCS the amount of funds representing the difference between the Target Net Income and the actual amount of
net income shown on WCS’s Form K-1, as a distribution from Sanara Pulsar to WCS. For each of the years 2021 through 2024 the Target
Net Income was to increase by 10%. In April 2022, the Company paid WCS $220,000 related to the fiscal 2021 Form K-1 and in December 2022,
the Company accrued an additional payment of $242,000 related to the projected fiscal 2022 Form K-1. Sanara Pulsar, which had minimal
sales since its inception, was dissolved effective December 2022, and accordingly, there will be no additional payments made beyond the
accrued payment.
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v3.23.3
SHAREHOLDERS’ EQUITY
|
9 Months Ended |
Sep. 30, 2023 |
Equity [Abstract] |
|
SHAREHOLDERS’ EQUITY |
NOTE
11 – SHAREHOLDERS’ EQUITY
Common
Stock
At
the Company’s Annual Meeting of Shareholders held in July 2020, the Company approved the Restated 2014 Omnibus Long Term Incentive
Plan (the “LTIP Plan”) in which the Company’s directors, officers, employees and consultants are eligible to participate.
A total of 587,465 shares had been issued under the LTIP Plan and 1,412,535 were available for issuance as of September 30, 2023.
In
April 2022, the Company closed a merger transaction with Precision Healing pursuant to which Precision Healing became a wholly owned
subsidiary of the Company. Pursuant to the terms of the merger agreement, holders of Precision Healing common stock and preferred stock,
other than the Company, were entitled to receive closing consideration, consisting of $125,966 in cash consideration, which was paid
to stockholders who were not accredited investors, 165,738 shares of the Company’s common stock, which was paid only to accredited
investors, and the payment in cash of approximately $0.6 million of transaction expenses of Precision Healing. The Company recorded the
issuance of the 165,738 shares to accredited investors and cash payments to nonaccredited investors based on the closing price per share
of the Company’s common stock on April 4, 2022, which was $30.75.
Upon
the closing of the merger, the Precision Healing outstanding options previously granted under the Precision Healing Plan converted, pursuant
to their terms, into options to acquire an aggregate of 144,191 shares of Company common stock with a weighted average exercise price
of $10.71 per share. These options expire between August 2030 and April 2031. In addition, outstanding and unexercised Precision Healing
warrants converted into rights to receive warrants to purchase (i) 4,424 shares of Company common stock with an initial exercise price
of $7.32 per share and an expiration date of April 22, 2031, and (ii) 12,301 shares of the Company’s common stock with an initial
exercise price of $12.05 per share and an expiration date of August 10, 2030. Concurrent with the assumption of the Precision Healing
Plan, the Company terminated the ability to offer future awards under the Precision Healing Plan.
Pursuant
to the merger agreement, upon the achievement of certain performance thresholds, the securityholders of Precision Healing, including
the holders of options and warrants to purchase Precision Healing common stock and certain persons promised options to purchase Precision
Healing common stock, are also entitled to receive payments of up to $10.0 million, which was accounted for as contingent consideration
pursuant to ASC 805. The earnout consideration is payable in cash or, at the Company’s election, is payable to accredited investors
in shares of Company common stock at a price per share equal to the greater of (i) $27.13 or (ii) the average closing price of Company
common stock for the 20 trading days prior to the date such earnout consideration is due and payable. Pursuant to the merger agreement,
a minimum percentage of the earnout consideration may be required to be issued to accredited investors in shares of Company common stock
for tax purposes. The amount and composition of the portion of earnout consideration payable is subject to adjustment and offsets as
set forth in the merger agreement. See Note 3 for more information regarding the merger with Precision Healing.
In
July 2022, the Company closed the Scendia acquisition pursuant to which Scendia became a wholly owned subsidiary of the Company. Pursuant
to the purchase agreement, the aggregate consideration at closing for the acquisition was approximately $7.6 million, subject to customary
post-closing adjustments. The consideration consisted of (i) approximately $1.6 million of cash, subject to certain adjustments, and
(ii) 291,686 shares of common stock of the Company. Pursuant to the purchase agreement, at closing, the Company withheld 94,798 Indemnity
Holdback Shares, which such Indemnity Holdback Shares were withheld to the extent provided in the purchase agreement to satisfy Phillips’
indemnification obligations and subsequently issued and released to Phillips in July 2023.
In
addition to the cash consideration and the stock consideration, the purchase agreement provides that Phillips is entitled to receive
two potential earnout payments, payable on an annual basis, not to exceed $10.0 million in the aggregate, which was accounted for as
contingent consideration pursuant to ASC 805. The earnout consideration is payable to Phillips in cash or, at the Company’s election,
in up to 486,145 shares of the Company’s common stock upon the achievement of certain performance thresholds relating to net revenue
attributable to sales of Scendia products during the two-year period following the closing. The Company made the first earnout payment
of approximately $693,000 in cash in August 2023. See Note 4 for more information regarding the acquisition of Scendia.
In
February 2023, the Company entered into a Controlled Equity Offering SM Sales Agreement (the “Sales Agreement”)
with Cantor Fitzgerald & Co., as sales agent (“Cantor”), pursuant to which the Company may offer and sell from time to
time, to or through Cantor, shares of the Company’s common stock having an aggregate offering price of up to $75,000,000.
Sales
of the shares, if any, pursuant to the Sales Agreement, may be made in sales deemed to be an “at the market offering” as
defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. Upon delivery of a placement notice and subject to
the terms and conditions of the Sales Agreement, Cantor agreed to use commercially reasonable efforts consistent with its normal trading
and sales practices, applicable state and federal law, rules and regulations and the rules of The Nasdaq Capital Market to sell the shares
from time to time based upon the Company’s instructions, including any price, time period or size limits specified by the Company.
The Company has no obligation to sell any of the shares under the Sales Agreement and may at any time suspend or terminate the offering
of its common stock pursuant to the Sales Agreement upon notice to Cantor and subject to other conditions. Cantor’s obligations
to sell the shares under the Sales Agreement are subject to satisfaction of certain conditions, including customary closing conditions.
Pursuant to the Sales Agreement, the Company will pay Cantor a commission of 3.0% of the aggregate gross proceeds from each sale of the
shares.
During
the three months ended September 30, 2023, the Company did not sell any shares of common stock pursuant to the Sales Agreement. During
the nine months ended September 30, 2023, the Company sold an aggregate of 26,143 shares of common stock for gross proceeds of approximately
$1,066,000 and net proceeds of approximately $1,034,000 pursuant to the Sales Agreement.
On
August 1, 2023, the Company closed the Applied Asset Purchase. The Applied Purchased Assets were purchased for an initial aggregate
purchase price of $15.25
million, consisting of (i) the Cash Closing Consideration, (ii) the Stock Closing Consideration and (iii) the Installment
Payments.
Restricted
Stock Awards
During
the nine months ended September 30, 2023, the Company issued restricted stock awards under the LTIP Plan which are subject to certain
vesting provisions and other terms and conditions set forth in each recipient’s respective restricted stock agreement. The Company
granted and issued 107,797 shares, net of forfeitures, of restricted common stock to employees, directors, and certain advisors of the
Company under the LTIP Plan during the nine months ended September 30, 2023. The fair value of these awards was $4,287,777 based on the
closing price of the Company’s common stock on the respective grant dates, which will be recognized as compensation expense on
a straight-line basis over the vesting period of the awards.
Share-based
compensation expense of $857,526 and $683,202 was recognized in “Selling, general and administrative expenses” in the accompanying
Consolidated Statements of Operations during the three months ended September 30, 2023 and 2022, respectively, and $2,582,163 and $1,971,537
was recognized during the nine months ended September 30, 2023 and 2022, respectively.
At
September 30, 2023, there was $3,980,624 of total unrecognized share-based compensation expense related to unvested share-based equity
awards. Unrecognized share-based compensation expense is expected to be recognized over a weighted-average period of 1.0 years.
Below
is a summary of restricted stock activity for the nine months ended September 30, 2023:
SUMMARY
OF RESTRICTED STOCK ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
Shares | | |
Weighted Average Grant Date Fair Value | |
Nonvested at beginning of period | |
| 181,102 | | |
$ | 22.89 | |
Granted | |
| 118,912 | | |
| 39.14 | |
Vested | |
| (129,342 | ) | |
| 22.84 | |
Forfeited | |
| (11,115 | ) | |
| 32.96 | |
Nonvested at September 30, 2023 | |
| 159,557 | | |
$ | 34.27 | |
Stock
Options
A
summary of the status of outstanding stock options at September 30, 2023 and changes during the nine months then ended is presented below:
SCHEDULE OF STOCK OPTION ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Options | | |
Price | | |
Contract
Life | |
Outstanding at beginning of period | |
| 146,191 | | |
$ | 10.65 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| (50,318 | ) | |
| 11.58 | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
Warrants
A
summary of the status of outstanding warrants to purchase common stock at September 30, 2023 and changes during the nine months then
ended is presented below:
SCHEDULE OF WARRANTS TO PURCHASE COMMON STOCK
| |
For the Nine Months Ended
September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Warrants | | |
Price | | |
Contract Life | |
Outstanding at beginning of period | |
| 16,725 | | |
$ | 10.80 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| - | | |
| - | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
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v3.23.3
INCOME TAXES
|
9 Months Ended |
Sep. 30, 2023 |
Income Tax Disclosure [Abstract] |
|
INCOME TAXES |
NOTE
12 – INCOME TAXES
As
discussed in Notes 3 and 4, the Company recognized net deferred tax liabilities associated with the Precision Healing merger and the
Scendia acquisition. Prior to consideration of these deferred tax liabilities, the Company had net deferred tax assets in excess of the
deferred tax liabilities being recognized, however, a 100% valuation allowance had previously been provided against the Company’s
net deferred tax assets. As a result of the recording of the net deferred tax liabilities related to the Precision Healing merger and
the Scendia acquisition, the Company reviewed the valuation allowance and determined that it should be reduced by the amount of the deferred
tax liabilities that were recognized. This resulted in an income tax benefit of $1,702,890 and $5,844,796 in the three and nine months
ended September 30, 2022, respectively.
|
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- DefinitionThe entire disclosure for income taxes. Disclosures may include net deferred tax liability or asset recognized in an enterprise's statement of financial position, net change during the year in the total valuation allowance, approximate tax effect of each type of temporary difference and carryforward that gives rise to a significant portion of deferred tax liabilities and deferred tax assets, utilization of a tax carryback, and tax uncertainties information.
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v3.23.3
RELATED PARTIES
|
9 Months Ended |
Sep. 30, 2023 |
Related Party Transactions [Abstract] |
|
RELATED PARTIES |
NOTE
13 – RELATED PARTIES
CellerateRX
Surgical Sublicense Agreement
The
Company has an exclusive, world-wide sublicense to distribute CellerateRX Surgical and HYCOL products into the surgical and wound care
markets from an affiliate of The Catalyst Group, Inc. (“Catalyst”), CGI Cellerate RX, which, prior to the Applied Asset Purchase,
licensed the rights to CellerateRX Surgical and HYCOL from Applied. Sales of CellerateRX Surgical comprised the substantial majority
of the Company’s sales during the nine months ended September 30, 2023 and 2022. In January 2021, the Company amended the term
of the Sublicense Agreement to extend the term to May 17, 2050, with automatic successive one-year renewals so long as annual net sales
of the licensed products exceed $1,000,000. The Company pays royalties based on the annual Net Sales of licensed products (as defined
in the Sublicense Agreement) consisting of 3% of all collected Net Sales each year up to $12,000,000, 4% of all collected Net Sales each
year that exceed $12,000,000 up to $20,000,000, and 5% of all collected Net Sales each year that exceed $20,000,000.
As
discussed further in Note 5, on August 1, 2023, the Company purchased certain assets from Applied, including the underlying
intellectual property of, as well as the rights to manufacture and sell, CellerateRX Surgical and HYCOL products. In connection with
the Applied Asset Purchase, Applied assigned its license agreement with CGI Cellerate RX to SMAT. Since the Closing, Sanara
indirectly makes intercompany royalty payments to SMAT at the same rate as set forth in the Sublicense Agreement. Ronald T. Nixon,
the Company’s Executive Chairman, is the founder and managing partner of Catalyst.
Product
License Agreements
In
July 2019, the Company executed a license agreement with Rochal, a related party, whereby the Company acquired an exclusive world-wide
license to market, sell and further develop antimicrobial products for the prevention and treatment of microbes on the human body utilizing
certain Rochal patents and pending patent applications. Currently, the products covered by the BIAKŌS License Agreement are BIAKŌS
Antimicrobial Wound Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser. Both products are 510(k) cleared. Mr. Nixon is a director
of Rochal, and indirectly a significant shareholder of Rochal, and through the potential exercise of warrants, a majority shareholder
of Rochal. Another one of the Company’s directors is also a significant shareholder and the current Chair of the board of directors
of Rochal.
In
October 2019, the Company executed the ABF License Agreement with Rochal whereby the Company acquired an exclusive world-wide license
to market, sell and further develop certain antimicrobial barrier film and skin protectant products for use in the human health care
market utilizing certain Rochal patents and pending patent applications. Currently, the products covered by the ABF License Agreement
are CuraShield Antimicrobial Barrier Film and a no sting skin protectant product.
In
May 2020, the Company executed a product license agreement with Rochal, whereby the Company acquired an exclusive world-wide license
to market, sell and further develop a debrider for human medical use to enhance skin condition or treat or relieve skin disorders, excluding
uses primarily for beauty, cosmetic, or toiletry purposes.
See
Note 10 for more information on these product license agreements.
Consulting
Agreement
Concurrent
with the Rochal asset purchase, in July 2021, the Company entered into a consulting agreement with Ann Beal Salamone pursuant to which
Ms. Salamone agreed to provide the Company with consulting services with respect to, among other things, writing new patents, conducting
patent intelligence, and participating in certain grant and contract reporting. In consideration for the consulting services to be provided
to the Company, Ms. Salamone is entitled to receive an annual consulting fee of $177,697, with payments to be paid once per month. The
consulting agreement has an initial term of three years, unless earlier terminated by the Company, and is subject to renewal. Ms. Salamone
is a director of the Company and is a significant shareholder and the current Chair of the board of directors of Rochal.
Catalyst
Transaction Advisory Services Agreement
In
March 2023, the Company entered into a Transaction Advisory Services Agreement (the “Catalyst Services Agreement”) effective
March 1, 2023 with Catalyst, a related party. Pursuant to the Catalyst Services Agreement, Catalyst, by and through its directors, officers,
employees and affiliates that are not simultaneously serving as directors, officers or employees of the Company (collectively, the “Covered
Persons”), agreed to perform certain transaction advisory, business and organizational strategy, finance, marketing, operational
and strategic planning, relationship access and corporate development services for the Company in connection with any merger, acquisition,
recapitalization, divestiture, financing, refinancing, or other similar transaction in which the Company may be, or may consider becoming,
involved, and any such additional services as mutually agreed upon in writing by and between Catalyst and the Company (the “Catalyst
Services”).
Pursuant
to the Catalyst Services Agreement, the Company agreed to reimburse Catalyst for (i) compensation actually paid by Catalyst to any of
the Covered Persons at a rate no more than a rate consistent with industry practice for the performance of services similar to the Catalyst
Services, as documented in reasonably sufficient detail, and (ii) all reasonable out-of-pocket costs and expenses payable to unaffiliated
third parties, as documented in customary expense reports, as each of (i) and (ii) is incurred in connection with the Catalyst Services
rendered under the Catalyst Services Agreement, with all reimbursements being contingent upon the prior approval of the Audit Committee
of the Company’s Board of Directors. The Company incurred $44,032
and $117,018
of costs pursuant to the Catalyst Services
Agreement in the three and nine months ended September 30, 2023, respectively.
|
X |
- DefinitionThe entire disclosure for related party transactions. Examples of related party transactions include transactions between (a) a parent company and its subsidiary; (b) subsidiaries of a common parent; (c) and entity and its principal owners; and (d) affiliates.
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v3.23.3
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Policies)
|
9 Months Ended |
Sep. 30, 2023 |
Accounting Policies [Abstract] |
|
Principles of Consolidation and Basis of Presentation |
Principles
of Consolidation and Basis of Presentation
The
accompanying unaudited consolidated financial statements include the accounts of Sanara MedTech Inc. and its wholly owned and majority-owned
subsidiaries, as well as other entities in which the Company has a controlling financial interest. All significant intercompany profits,
losses, transactions and balances have been eliminated in consolidation. Certain prior year amounts have been reclassified to conform
to the current year presentation.
The
accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles
for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include
all the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. In the
opinion of management of the Company, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation
have been included. Operating results for interim periods are not necessarily indicative of the results that may be expected for the
full year period. These financial statements and notes should be read in conjunction with the financial statements for each of the two
years ended December 31, 2022 and 2021, which are included in the Company’s most recent Annual Report on Form 10-K.
|
Use of Estimates |
Use
of Estimates
The
preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates
and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date
of the consolidated financial statements, and the reported revenue and expenses during the reporting period. However, actual results
could differ from those estimates and there may be changes to the Company’s estimates in future periods.
|
Cash and Cash Equivalents |
Cash
and Cash Equivalents
The
Company considers all highly liquid investments purchased with an original maturity of three months or less to be cash equivalents.
|
Income/Loss Per Share |
Income/Loss
Per Share
The
Company computes income/loss per share in accordance with Accounting Standards Codification (“ASC”) Topic 260, Earnings per
Share, which requires the Company to present basic and diluted income per share when the effect is dilutive. Basic income per share is
computed by dividing income available to common shareholders by the weighted average number of shares of common stock outstanding. Diluted
income per share is computed similarly to basic income per share, except that the denominator is increased to include the number of additional
shares of common stock that would have been outstanding if the potential shares of common stock had been issued and if the additional
shares of common stock were dilutive. All common stock equivalents were excluded from the calculations for the periods presented as their
inclusion would have been anti-dilutive during the three and nine months ended September 30, 2023 and 2022 due to the Company’s
net loss.
The
following table summarizes the shares of common stock that were potentially issuable but were excluded from the computation of diluted
net loss per share for the nine months ended September 30, 2023 and 2022, as such shares would have had an anti-dilutive effect:
SCHEDULE
OF COMPUTATION OF DILUTED NET LOSS PER SHARE
| |
2023 | | |
2022 | |
| |
As of September 30, | |
| |
2023 | | |
2022 | |
Stock options (a) | |
| 95,873 | | |
| 155,691 | |
Warrants (b) | |
| 16,725 | | |
| 16,725 | |
Unvested restricted stock | |
| 159,557 | | |
| 192,215 | |
Anti-dilutive securities | |
| 159,557 | | |
| 192,215 | |
(a) | Shares underlying
stock options assumed pursuant to the merger agreement with Precision Healing, Inc. (“Precision Healing”) in April 2022.
See Note 3 for more information regarding the Precision Healing merger. |
(b) | Shares underlying
warrants assumed pursuant to the merger agreement with Precision Healing in April 2022. See Note 3 for more information regarding the
Precision Healing merger. |
|
Revenue Recognition |
Revenue
Recognition
The
Company recognizes revenue in accordance with ASC Topic 606, Revenue from Contracts with Customers (“ASC 606”). Revenues
are recognized when a purchase order is received from the customer and control of the promised goods or services is transferred to the
customer in an amount that reflects the consideration the Company expects to be entitled to receive in exchange for transferring those
goods or services. Revenue is recognized based on the following five-step model:
-
Identification of the contract with a customer
-
Identification of the performance obligations in the contract
-
Determination of the transaction price
-
Allocation of the transaction price to the performance obligations in the contract
-
Recognition of revenue when, or as, the Company satisfies a performance obligation
Details
of this five-step process are as follows:
Identification
of the contract with a customer
Customer
purchase orders are generally considered to be contracts under ASC 606. Purchase orders typically identify the specific terms of products
to be delivered, create the enforceable rights and obligations of both parties and result in commercial substance. No other forms of
contract revenue recognition, such as the completed contract or percentage of completion methods, were utilized by the Company in either
2023 or 2022.
Performance
obligations
The
Company’s performance obligation is generally limited to delivery of the requested items to its customers at the agreed upon quantities
and prices.
Determination
and allocation of the transaction price
The
Company has established prices for its products. These prices are effectively agreed to when customers place purchase orders with the
Company. Rebates and discounts, if any, are recognized in full at the time of sale as a reduction of net revenue. Allocation of transaction
prices is not necessary where only one performance obligation exists.
Recognition
of revenue as performance obligations are satisfied
Product
revenues are recognized when a purchase order is received from the customer, the products are delivered and control of the goods and
services passes to the customer.
Disaggregation
of Revenue
Revenue
streams from product sales and royalties are summarized below for the three and nine months ended September 30, 2023 and 2022.
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Soft tissue repair products | |
$ | 13,634,316 | | |
$ | 10,969,271 | | |
$ | 39,756,539 | | |
$ | 28,296,919 | |
Bone fusion products | |
| 2,340,382 | | |
| 2,025,050 | | |
| 7,392,740 | | |
| 2,078,903 | |
Royalty revenue | |
| 50,250 | | |
| 50,250 | | |
| 150,750 | | |
| 150,750 | |
Total Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
The
Company recognizes royalty revenue from a development and license agreement with BioStructures, LLC. The Company records revenue each
calendar quarter as earned per the terms of the agreement, which stipulates the Company will receive quarterly royalty payments of at
least $50,250. Under the terms of the development and license agreement, royalties of 2.0% are recognized on sales of products containing
the Company’s patented resorbable bone hemostasis. The minimum annual royalty due to the Company is $201,000 per year through the
end of 2023. These royalties are payable in quarterly installments of $50,250. To date, royalties related to this development and license
agreement have not exceeded the annual minimum of $201,000 ($50,250 per quarter).
|
Accounts Receivable Allowances |
Accounts
Receivable Allowances
Accounts
receivable are typically due within 30 days of invoicing. The Company establishes an allowance for doubtful accounts to provide for an
estimate of accounts receivable which are not expected to be collectible. The Company bases the allowance on an assessment of customer
creditworthiness, historical payment experience, the age of outstanding receivables and other information as applicable. The Company
recorded bad debt expense of $128,061 and $25,000 during the three months ended September 30, 2023 and 2022, respectively, and $214,061
and $220,000 during the nine months ended September 30, 2023 and 2022, respectively. The allowance for doubtful accounts was $511,089
at September 30, 2023 and $265,089 at December 31, 2022. The Company also establishes other allowances to provide for estimated customer
rebates and other expected customer deductions. These allowances totaled $5,297 at September 30, 2023 and $4,761 at December 31, 2022.
If circumstances related to customers change, estimates of the recoverability of receivables would be further adjusted.
|
Inventories |
Inventories
Inventories are stated at the lower
of cost or net realizable value, with cost computed on a first-in, first-out basis. Inventories consist primarily of finished goods,
and also include an immaterial amount of raw materials and related packaging components. The Company recorded inventory obsolescence
expense of $152,701
and $129,689
for the three months ended September 30, 2023 and 2022, respectively, and $222,691
and $289,406
for the nine months ended September 30, 2023 and 2022, respectively. The allowance for obsolete and slow-moving inventory had a
balance of $327,492
at September 30, 2023, and $523,832 at
December 31, 2022.
|
Property and Equipment |
Property
and Equipment
Property
and equipment are stated at cost, less accumulated depreciation. Depreciation is recorded using the straight-line method over the estimated
useful lives of the related assets, ranging from two to ten years. Below is a summary of property and equipment for the periods presented:
SCHEDULE OF PROPERTY AND EQUIPMENT
| |
Useful | | |
September 30, | | |
December 31, | |
| |
Life | | |
2023 | | |
2022 | |
Computers | |
| 3-5 years | | |
$ | 194,788 | | |
$ | 172,154 | |
Office equipment | |
| 3-7 years | | |
| 154,280 | | |
| 87,225 | |
Furniture and fixtures | |
| 5-10 years | | |
| 323,755 | | |
| 258,414 | |
Leasehold improvements | |
| 2-5 years | | |
| 107,983 | | |
| 19,631 | |
Internal use software | |
| 5 years | | |
| 1,618,998 | | |
| 1,618,998 | |
Property and equipment, gross | |
| | | |
| 2,399,804 | | |
| 2,156,422 | |
Less accumulated depreciation | |
| | | |
| (1,072,748 | ) | |
| (739,986 | ) |
Property and equipment, net | |
| | | |
$ | 1,327,056 | | |
$ | 1,416,436 | |
Depreciation
expense related to property and equipment was $116,596 and $106,347 for the three months ended September 30, 2023 and 2022, respectively,
and $332,762 and $300,655 for the nine months ended September 30, 2023 and 2022, respectively.
|
Internal Use Software |
Internal
Use Software
The
Company accounts for costs incurred to develop or acquire computer software for internal use in accordance with ASC Topic 350-40, Intangibles
– Goodwill and Other. The Company capitalizes the costs incurred during the application development stage, which generally includes
third-party developer fees to design the software configuration and interfaces, coding, installation and testing.
The
Company begins capitalization of qualifying costs when both the preliminary project stage is completed and management has authorized
further funding for the completion of the project. Costs incurred during the preliminary project stage along with post implementation
stages of internal-use computer software are expensed as incurred. The Company also capitalizes costs related to specific upgrades and
enhancements when it is probable the expenditures will result in additional functionality. Capitalized development costs are classified
as “Property and equipment, net” in the Consolidated Balance Sheets and are depreciated over the estimated useful life of the
software, which is generally five years.
|
Goodwill |
Goodwill
The
excess of purchase price over the fair value of identifiable net assets acquired in business combinations is recorded as goodwill. As
of September 30, 2023, all the Company’s goodwill relates to the acquisition of Scendia Biologics, LLC (“Scendia”)
(see Note 4). Goodwill has an indefinite useful life and is not amortized. Goodwill is tested annually as of December 31 for impairment,
or more frequently if circumstances indicate impairment may have occurred. The Company may first perform a qualitative assessment to
determine if it is more likely than not that the fair value of the reporting unit is less than the respective carrying value. If it is
determined that it is more likely than not that a reporting unit’s fair value is less than its carrying value, then the Company
will determine the fair value of the reporting unit and record an impairment charge for the difference between fair value and carrying
value (not to exceed the carrying amount of goodwill). No impairment was recorded during the nine months ended September 30, 2023.
|
Intangible Assets |
Intangible
Assets
Intangible
assets are stated at cost of acquisition less accumulated amortization and impairment loss, if any. Cost of acquisition includes the
purchase price and any cost directly attributable to bringing the asset to its working condition for the intended use. The Company amortizes
its finite-lived intangible assets on a straight-line basis over the estimated useful life of the respective assets which is generally
the life of the related patents or licenses, seven years for customer relationships and five years for assembled workforces. See Note
6 for more information on intangible assets.
|
Impairment of Long-Lived Assets |
Impairment
of Long-Lived Assets
Long-lived
assets, including certain identifiable intangibles held and to be used by the Company, are reviewed for impairment whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The Company continuously evaluates
the recoverability of its long-lived assets based on estimated future cash flows and the estimated liquidation value of such long-lived
assets and provides for impairment if such undiscounted cash flows are insufficient to recover the carrying amount of the long-lived
assets. If impairment exists, an adjustment is made to write the asset down to its fair value, and a loss is recorded as the difference
between the carrying value and fair value. Fair values are determined based on quoted market values, undiscounted cash flows or internal
and external appraisals, as applicable. Assets to be disposed of are carried at the lower of carrying value or estimated fair value less
cost to sell. No impairment was recorded during the nine months ended September 30, 2023 and 2022.
|
Investments in Equity Securities |
Investments
in Equity Securities
The
Company’s equity investments consist of nonmarketable equity securities in privately held companies without readily determinable
fair values. Unless accounted for under the equity method of accounting, the investments are reported at cost minus impairment, if any,
plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the
same issuer.
The
Company applies the equity method of accounting to investments when it has significant influence, but not controlling interest, in the
investee. Judgment regarding the level of influence over each equity method investment includes considering key factors such as ownership
interest, representation on the board of directors, participation in policy-making decisions and material intercompany transactions.
The Company’s proportionate share of the net income (loss) resulting from these investments is reported under the line item captioned
“Share of losses from equity method investment” in the Company’s Consolidated Statements of Operations. The Company’s
equity method investment is adjusted each period for the Company’s share of the investee’s income or loss and dividend paid,
if any. The Company classifies distributions received from its equity method investment using the cumulative earnings approach in the
Company’s Consolidated Statements of Cash Flows. As a result of the Precision Healing merger in April 2022 (see Note 3), the
Company did not have any investments which are recorded applying the equity method of accounting as of September 30, 2023.
The
Company has reviewed the carrying value of its investments and has determined there was no impairment or observable price changes as
of and for the nine months ended September 30, 2023 or 2022.
|
Fair Value Measurement |
Fair
Value Measurement
As
defined in ASC Topic 820, Fair Value Measurement (“ASC 820”), fair value is the price that would be received to sell an asset
or paid to transfer a liability in an orderly transaction between market participants at the measurement date (exit price). The Company
utilizes market data or assumptions that market participants would use in pricing the asset or liability, including assumptions about
risk and the risks inherent in the inputs to the valuation technique. These inputs can be readily observable, market corroborated, or
generally unobservable. ASC 820 establishes a fair value hierarchy that prioritizes the inputs used to measure fair value. The hierarchy
gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurement) and
the lowest priority to unobservable inputs (Level 3 measurement). This fair value measurement framework applies at both initial and subsequent
measurement.
The
three levels of the fair value hierarchy defined by ASC 820 are as follows:
Level
1 – Quoted prices are available in active markets for identical assets or liabilities as of the reporting date. Active markets
are those in which transactions for the asset or liability occur in sufficient frequency and volume to provide pricing information on
an ongoing basis. Level 1 primarily consists of financial instruments such as exchange-traded derivatives, marketable securities and
listed equities.
Level
2 – Pricing inputs are other than quoted prices in active markets included in Level 1, which are either directly or indirectly
observable as of the reported date. Level 2 includes those financial instruments that are valued using models or other valuation methodologies.
These models are primarily industry-standard models that consider various assumptions, including quoted forward prices for commodities,
time value, volatility factors, and current market and contractual prices for the underlying instruments, as well as other relevant economic
measures. Substantially all these assumptions are observable in the marketplace throughout the full term of the instrument, can be derived
from observable data or are supported by observable levels at which transactions are executed in the marketplace. Instruments in this
category generally include nonexchange-traded derivatives such as commodity swaps, interest rate swaps, options and collars.
Level
3 – Pricing inputs include significant inputs that are generally less observable from objective sources. These inputs may be used
with internally developed methodologies that result in management’s best estimate of fair value.
The
carrying amounts of cash, accounts receivable, accounts payable and accrued expenses, other than acquisition-related accrued expenses,
approximate fair value because of the short-term nature of these instruments. The fair value of acquisition-related accrued expenses is categorized
as Level 2 of the fair value hierarchy. The value of these instruments has been estimated using discounted cash flow analysis based on
the Company’s incremental borrowing rate. The carrying value of the Company’s debt, which has
variable interest rates determined each month, approximates fair value based on instruments with similar terms (Level 2 inputs). The
fair value of the contingent earnout consideration and the acquisition date fair value of goodwill
and intangibles related to the acquisitions discussed in Notes 3, 4 and 5 are based on Level 3 inputs.
Liabilities
for contingent consideration are measured at fair value each reporting period, with the acquisition-date fair value included as part
of the consideration transferred. Subsequent changes in fair value are reported under the line item captioned “Change in fair value
of earnout liabilities” in the Company’s Consolidated Statements of Operations. The current year changes in fair value of earnout liabilities below are
as a result of a decrease in the estimated fair value of the earnout liabilities established at the time of the Company’s Precision Healing and
Scendia acquisitions. The following table sets forth a summary
of the changes in fair value for the Level 3 contingent earnout consideration.
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
|
Income Taxes |
Income
Taxes
Income
taxes are accounted for under the asset and liability method, whereby deferred income taxes are recorded for temporary differences between
financial statement carrying amounts and the tax basis of assets and liabilities. Deferred tax assets and liabilities reflect the tax
rates expected to be in effect for the years in which the differences are expected to reverse. A valuation allowance is provided if it
is more likely than not that some or all the deferred tax asset will not be realized.
|
Stock-based Compensation |
Stock-based
Compensation
The
Company accounts for stock-based compensation to employees and nonemployees in accordance with Accounting Standards Update (“ASU”)
2018-07, Compensation – Stock Compensation (Topic 718). Stock-based compensation is measured at the grant date, based on the fair
value of the award, and is recognized as expense over the stipulated vesting period, if any. The Company estimates the fair value of
stock-based payments using the Black-Scholes option-pricing model for common stock options and warrants, and the closing price of the
Company’s common stock for grants of common stock, including restricted stock awards.
|
Research and Development Costs |
Research
and Development Costs
Research
and development (“R&D”) expenses consist of personnel-related expenses, including salaries and benefits for all personnel
directly engaged in R&D activities, contracted services, materials, prototype expenses and allocated overhead which is comprised
of lease expense and other facilities-related costs. R&D expenses include costs related to enhancements to the Company’s currently
available products and additional investments in the product, services and technologies development pipeline. The Company expenses R&D
costs as incurred.
|
Recently Adopted Accounting Pronouncements |
Recently
Adopted Accounting Pronouncements
In
June 2016, the Financial Accounting Standards Board issued ASU 2016-13, Financial Instruments - Credit Losses (Topic 326). This update
amends the impairment model by requiring entities to use a forward-looking approach based on expected losses to estimate credit losses
for most financial assets and certain other instruments that are not measured at fair value through net income. The Company adopted the
new guidance effective January 1, 2023. The adoption did not have a material impact on the Company’s consolidated financial position,
results of operations or cash flows.
|
Recently Issued Accounting Pronouncements |
Recently
Issued Accounting Pronouncements
There
are no recently issued accounting pronouncements that have not yet been adopted that are expected to have a material effect on the Company’s
consolidated financial condition, results of operations or cash flows.
|
X |
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v3.23.3
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Accounting Policies [Abstract] |
|
SCHEDULE OF COMPUTATION OF DILUTED NET LOSS PER SHARE |
The
following table summarizes the shares of common stock that were potentially issuable but were excluded from the computation of diluted
net loss per share for the nine months ended September 30, 2023 and 2022, as such shares would have had an anti-dilutive effect:
SCHEDULE
OF COMPUTATION OF DILUTED NET LOSS PER SHARE
| |
2023 | | |
2022 | |
| |
As of September 30, | |
| |
2023 | | |
2022 | |
Stock options (a) | |
| 95,873 | | |
| 155,691 | |
Warrants (b) | |
| 16,725 | | |
| 16,725 | |
Unvested restricted stock | |
| 159,557 | | |
| 192,215 | |
Anti-dilutive securities | |
| 159,557 | | |
| 192,215 | |
(a) | Shares underlying
stock options assumed pursuant to the merger agreement with Precision Healing, Inc. (“Precision Healing”) in April 2022.
See Note 3 for more information regarding the Precision Healing merger. |
(b) | Shares underlying
warrants assumed pursuant to the merger agreement with Precision Healing in April 2022. See Note 3 for more information regarding the
Precision Healing merger. |
|
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES |
Revenue
streams from product sales and royalties are summarized below for the three and nine months ended September 30, 2023 and 2022.
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Soft tissue repair products | |
$ | 13,634,316 | | |
$ | 10,969,271 | | |
$ | 39,756,539 | | |
$ | 28,296,919 | |
Bone fusion products | |
| 2,340,382 | | |
| 2,025,050 | | |
| 7,392,740 | | |
| 2,078,903 | |
Royalty revenue | |
| 50,250 | | |
| 50,250 | | |
| 150,750 | | |
| 150,750 | |
Total Net Revenue | |
$ | 16,024,948 | | |
$ | 13,044,571 | | |
$ | 47,300,029 | | |
$ | 30,526,572 | |
|
SCHEDULE OF PROPERTY AND EQUIPMENT |
SCHEDULE OF PROPERTY AND EQUIPMENT
| |
Useful | | |
September 30, | | |
December 31, | |
| |
Life | | |
2023 | | |
2022 | |
Computers | |
| 3-5 years | | |
$ | 194,788 | | |
$ | 172,154 | |
Office equipment | |
| 3-7 years | | |
| 154,280 | | |
| 87,225 | |
Furniture and fixtures | |
| 5-10 years | | |
| 323,755 | | |
| 258,414 | |
Leasehold improvements | |
| 2-5 years | | |
| 107,983 | | |
| 19,631 | |
Internal use software | |
| 5 years | | |
| 1,618,998 | | |
| 1,618,998 | |
Property and equipment, gross | |
| | | |
| 2,399,804 | | |
| 2,156,422 | |
Less accumulated depreciation | |
| | | |
| (1,072,748 | ) | |
| (739,986 | ) |
Property and equipment, net | |
| | | |
$ | 1,327,056 | | |
$ | 1,416,436 | |
|
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION |
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
|
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v3.23.3
PRECISION HEALING MERGER (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
|
Precision Healing Inc [Member] |
|
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATIONS |
The
total purchase consideration as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity
Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 165,738 | | |
$ | 5,096,444 | |
Fair value of assumed options | |
| 144,191 | | |
| 4,109,750 | |
Fair value of assumed warrants | |
| 16,725 | | |
| 502,895 | |
Cash paid to nonaccredited investors | |
| | | |
| 125,370 | |
Cash paid for fractional shares | |
| | | |
| 596 | |
Carrying value of equity method investment in Precision Healing | |
| | | |
| 1,803,440 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,882,151 | |
Direct transaction costs | |
| | | |
| 1,061,137 | |
Total purchase consideration | |
| | | |
$ | 16,581,783 | |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 32,202 | |
Net working capital (excluding cash) | |
| (308,049 | ) |
Noncontrolling interest in Sanara Biologics, LLC | |
| | |
Customer relationships | |
| | |
Fixed assets, net | |
| 9,228 | |
Deferred tax assets | |
| 278,661 | |
Intellectual property | |
| 20,325,469 | |
Assembled workforce | |
| 664,839 | |
Deferred tax liabilities | |
| (4,420,567 | ) |
Goodwill | |
| | |
Net assets acquired | |
$ | 16,581,783 | |
|
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v3.23.3
SCENDIA PURCHASE AGREEMENT (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
|
Scendia Biologics LLC [Member] |
|
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATIONS |
The
total purchase consideration, subject to typical post-closing adjustments, as determined by the Company was as follows:
SCHEDULE OF PURCHASE CONSIDERATIONS
Consideration | |
Equity Shares | | |
Dollar Value | |
Fair value of Sanara common shares issued | |
| 291,686 | | |
$ | 6,032,066 | |
Cash consideration | |
| | | |
| 1,562,668 | |
Fair value of contingent earnout consideration | |
| | | |
| 3,000,000 | |
Total purchase consideration | |
| | | |
$ | 10,594,734 | |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Cash | |
$ | 201,406 | |
Net working capital (excluding cash) | |
| 1,294,499 | |
Fixed assets, net | |
| 42,300 | |
Noncontrolling interest in Sanara Biologics, LLC | |
| 2,638 | |
Customer relationships | |
| 7,155,000 | |
Deferred tax liabilities | |
| (1,702,890 | ) |
Goodwill | |
| 3,601,781 | |
Net assets acquired | |
$ | 10,594,734 | |
|
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v3.23.3
APPLIED ASSET PURCHASE (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION
| |
| | |
Balance at December 31, 2022 | |
$ | 7,166,691 | |
Additions | |
| 893,000 | |
Changes in fair value of earnout liabilities | |
| (1,494,910 | ) |
Settlements | |
| (692,795 | ) |
Balance at September 30, 2023 | |
$ | 5,871,986 | |
|
Applied Asset Purchase [Member] |
|
Restructuring Cost and Reserve [Line Items] |
|
SCHEDULE OF PURCHASE CONSIDERATION |
The
total purchase consideration for the Applied Asset Purchase as determined by the Company was as follows:
SCHEDULE
OF PURCHASE CONSIDERATION
Consideration | |
Equity Shares | | |
Dollar Value | |
Cash Closing Consideration | |
| | | |
$ | 9,750,000 | |
Fair value of Stock Closing Consideration | |
| 73,809 | | |
| 3,089,645 | |
Fair value of Installment Payments | |
| | | |
| 2,040,808 | |
Cash paid for inventory | |
| | | |
| 30,007 | |
Fair value of Petito Services Agreement defined payments | |
| | | |
| 825,834 | |
Fair value of Petito Services Agreement contingent consideration | |
| | | |
| 893,000 | |
Direct transaction costs | |
| | | |
| 162,743 | |
Total purchase consideration | |
| | | |
$ | 16,792,037 | |
|
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED |
SCHEDULE
OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED
Description | |
Amount | |
Inventory | |
$ | 30,007 | |
Equipment | |
| 33,062 | |
Intellectual property | |
| 16,728,968 | |
Net assets acquired | |
$ | 16,792,037 | |
|
X |
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v3.23.3
INTANGIBLE ASSETS (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
SCHEDULE OF FINITE LIVED INTANGIBLE ASSETS |
The
carrying values of the Company’s intangible assets were as follows for the periods presented:
SCHEDULE OF FINITE LIVED INTANGIBLE ASSETS
| |
September 30, 2023 | | |
December 31, 2022 | |
| |
| | |
Accumulated | | |
| | |
| | |
Accumulated | | |
| |
| |
Cost | | |
Amortization | | |
Net | | |
Cost | | |
Amortization | | |
Net | |
Amortizable Intangible Assets: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Product licenses | |
$ | 4,793,879 | | |
$ | (1,246,115 | ) | |
$ | 3,547,764 | | |
$ | 4,793,879 | | |
$ | (980,583 | ) | |
$ | 3,813,296 | |
Patents and other IP | |
| 38,664,548 | | |
| (2,598,220 | ) | |
| 36,066,328 | | |
| 21,935,580 | | |
| (1,492,057 | ) | |
| 20,443,523 | |
Customer relationships and other | |
| 7,947,332 | | |
| (1,569,958 | ) | |
| 6,377,374 | | |
| 7,947,332 | | |
| (694,171 | ) | |
| 7,253,161 | |
Total | |
$ | 51,405,759 | | |
$ | (5,414,293 | ) | |
$ | 45,991,466 | | |
$ | 34,676,791 | | |
$ | (3,166,811 | ) | |
$ | 31,509,980 | |
|
SCHEDULE OF FUTURE AMORTIZATION EXPENSE |
SCHEDULE OF FUTURE AMORTIZATION EXPENSE
| |
| | |
Remainder of 2023 | |
$ | 974,018 | |
2024 | |
| 3,896,070 | |
2025 | |
| 3,896,070 | |
2026 | |
| 3,878,815 | |
2027 | |
| 3,764,962 | |
2028 | |
| 3,731,721 | |
Thereafter | |
| 25,849,810 | |
Total | |
$ | 45,991,466 | |
|
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v3.23.3
INVESTMENTS IN EQUITY SECURITIES (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Schedule of Investments [Abstract] |
|
SCHEDULE OF INVESTMENTS |
The
following summarizes the Company’s investments for the periods presented:
SCHEDULE
OF INVESTMENTS
| |
September
30, 2023 | | |
December
31, 2022 | |
| |
| Carrying
Amount | | |
| Economic
Interest | | |
| Carrying
Amount | | |
| Economic
Interest | |
Equity
Method Investment | |
| | | |
| | | |
| | | |
| | |
Precision
Healing Inc. | |
$ | - | | |
| - | % | |
$ | - | | |
| - | % |
| |
| | | |
| | | |
| | | |
| | |
Cost
Method Investments | |
| | | |
| | | |
| | | |
| | |
Direct
Dermatology, Inc. | |
| 1,000,000 | | |
| | | |
| 1,000,000 | | |
| | |
Pixalere
Healthcare Inc. | |
| 2,084,278 | | |
| | | |
| 2,084,278 | | |
| | |
Total
Cost Method Investments | |
| 3,084,278 | | |
| | | |
| 3,084,278 | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Total
Investments | |
$ | 3,084,278 | | |
| | | |
$ | 3,084,278 | | |
| | |
|
SCHEDULE OF LOSS FROM EQUITY METHOD INVESTMENT |
The
following summarizes the loss from the equity method investment reflected in the Consolidated Statements of Operations:
SCHEDULE OF LOSS FROM EQUITY METHOD INVESTMENT
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
Three
Months ended September 30, | | |
Nine
Months Ended September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Investment | |
| | |
| | |
| | |
| |
Precision
Healing Inc. | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
| |
| | | |
| | | |
| | | |
| | |
Total | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
Loss from equity method
investment | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | (379,633 | ) |
|
X |
- DefinitionTabular disclosure of equity method investments including, but not limited to, name of each investee or group of investments, percentage ownership, difference between recorded amount of an investment and the value of the underlying equity in the net assets, and summarized financial information.
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v3.23.3
OPERATING LEASES (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Operating Leases |
|
SCHEDULE OF OPERATING LEASE LIABILITY |
Maturity
of Operating Lease Liabilities
SCHEDULE OF OPERATING LEASE LIABILITY
| |
September 30,
2023 | |
Remainder of 2023 | |
$ | 116,285 | |
2024 | |
| 505,017 | |
2025 | |
| 532,053 | |
2026 | |
| 379,529 | |
2027 | |
| 297,947 | |
2028 | |
| 295,689 | |
Thereafter | |
| 604,049 | |
Total lease payments | |
| 2,730,569 | |
Less imputed interest | |
| (562,070 | ) |
Present Value of Lease Liabilities | |
$ | 2,168,499 | |
| |
| | |
Operating lease liabilities – current | |
| 322,206 | |
Operating lease liabilities – long-term | |
| 1,846,293 | |
|
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v3.23.3
DEBT AND CREDIT FACILITIES (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Debt And Credit Facilities |
|
SCHEDULE OF LONG-TERM DEBT |
The
table below presents the components of outstanding debt for the periods presented:
SCHEDULE
OF LONG-TERM DEBT
| |
September 30, 2023 | | |
December 31, 2022 | |
Term Loan | |
$ | 9,750,000 | | |
$ | - | |
Total debt | |
| 9,750,000 | | |
| - | |
Less: debt issuance costs, net of accumulated amortization of $2,055 and zero | |
| (59,603 | ) | |
| - | |
Long-term debt | |
| 9,690,397 | | |
| - | |
Less: current portion of debt | |
| 232,143 | | |
| - | |
Long-term debt, net of current portion | |
$ | 9,458,254 | | |
$ | - | |
|
SCHEDULE OF MATURITIES OUTSTANDING DEBT |
The
table below presents the aggregate maturities of the Company’s outstanding debt as of September 30, 2023:
SCHEDULE
OF MATURITIES OUTSTANDING DEBT
Year | |
Total | |
Remainder of 2023 | |
$ | - | |
2024 | |
| 580,357 | |
2025 | |
| 1,625,000 | |
2026 | |
| 1,950,000 | |
2027 | |
| 1,950,000 | |
2028 | |
| 3,644,643 | |
Thereafter | |
| - | |
Total debt | |
$ | 9,750,000 | |
|
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v3.23.3
SHAREHOLDERS’ EQUITY (Tables)
|
9 Months Ended |
Sep. 30, 2023 |
Equity [Abstract] |
|
SUMMARY OF RESTRICTED STOCK ACTIVITY |
Below
is a summary of restricted stock activity for the nine months ended September 30, 2023:
SUMMARY
OF RESTRICTED STOCK ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
Shares | | |
Weighted Average Grant Date Fair Value | |
Nonvested at beginning of period | |
| 181,102 | | |
$ | 22.89 | |
Granted | |
| 118,912 | | |
| 39.14 | |
Vested | |
| (129,342 | ) | |
| 22.84 | |
Forfeited | |
| (11,115 | ) | |
| 32.96 | |
Nonvested at September 30, 2023 | |
| 159,557 | | |
$ | 34.27 | |
|
SCHEDULE OF STOCK OPTION ACTIVITY |
A
summary of the status of outstanding stock options at September 30, 2023 and changes during the nine months then ended is presented below:
SCHEDULE OF STOCK OPTION ACTIVITY
| |
For the Nine Months Ended September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Options | | |
Price | | |
Contract
Life | |
Outstanding at beginning of period | |
| 146,191 | | |
$ | 10.65 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| (50,318 | ) | |
| 11.58 | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 95,873 | | |
$ | 10.16 | | |
| 7.1 | |
|
SCHEDULE OF WARRANTS TO PURCHASE COMMON STOCK |
A
summary of the status of outstanding warrants to purchase common stock at September 30, 2023 and changes during the nine months then
ended is presented below:
SCHEDULE OF WARRANTS TO PURCHASE COMMON STOCK
| |
For the Nine Months Ended
September 30, 2023 | |
| |
| | |
Weighted Average | | |
Weighted Average | |
| |
| | |
Exercise | | |
Remaining | |
| |
Warrants | | |
Price | | |
Contract Life | |
Outstanding at beginning of period | |
| 16,725 | | |
$ | 10.80 | | |
| | |
Granted or assumed | |
| - | | |
| - | | |
| | |
Exercised | |
| - | | |
| - | | |
| | |
Forfeited | |
| - | | |
| - | | |
| | |
Expired | |
| - | | |
| - | | |
| | |
Outstanding at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
| |
| | | |
| | | |
| | |
Exercisable at September 30, 2023 | |
| 16,725 | | |
$ | 10.80 | | |
| 7.0 | |
|
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v3.23.3
SCHEDULE OF COMPUTATION OF DILUTED NET LOSS PER SHARE (Details) - shares
|
9 Months Ended |
Sep. 30, 2023 |
Sep. 30, 2022 |
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] |
|
|
|
Anti-dilutive securities |
|
159,557
|
192,215
|
Equity Option [Member] |
|
|
|
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] |
|
|
|
Anti-dilutive securities |
[1] |
95,873
|
155,691
|
Warrant [Member] |
|
|
|
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] |
|
|
|
Anti-dilutive securities |
[2] |
16,725
|
16,725
|
Unvested Restricted Stock [Member] |
|
|
|
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] |
|
|
|
Anti-dilutive securities |
|
159,557
|
192,215
|
|
|
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v3.23.3
SCHEDULE OF REVENUE FROM PRODUCT SALES AND ROYALTIES (Details) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Product Information [Line Items] |
|
|
|
|
Total Net Revenue |
$ 16,024,948
|
$ 13,044,571
|
$ 47,300,029
|
$ 30,526,572
|
Soft Tissue Repair Products [Member] |
|
|
|
|
Product Information [Line Items] |
|
|
|
|
Total Net Revenue |
13,634,316
|
10,969,271
|
39,756,539
|
28,296,919
|
Bone Fusion Products [Member] |
|
|
|
|
Product Information [Line Items] |
|
|
|
|
Total Net Revenue |
2,340,382
|
2,025,050
|
7,392,740
|
2,078,903
|
Royalty [Member] |
|
|
|
|
Product Information [Line Items] |
|
|
|
|
Total Net Revenue |
$ 50,250
|
$ 50,250
|
$ 150,750
|
$ 150,750
|
X |
- DefinitionAmount, excluding tax collected from customer, of revenue from satisfaction of performance obligation by transferring promised good or service to customer. Tax collected from customer is tax assessed by governmental authority that is both imposed on and concurrent with specific revenue-producing transaction, including, but not limited to, sales, use, value added and excise.
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v3.23.3
SCHEDULE OF PROPERTY AND EQUIPMENT (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 2,399,804
|
$ 2,156,422
|
Less accumulated depreciation |
(1,072,748)
|
(739,986)
|
Property and equipment, net |
1,327,056
|
1,416,436
|
Computer Equipment [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 194,788
|
172,154
|
Computer Equipment [Member] | Minimum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
3 years
|
|
Computer Equipment [Member] | Maximum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
5 years
|
|
Office Equipment [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 154,280
|
87,225
|
Office Equipment [Member] | Minimum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
3 years
|
|
Office Equipment [Member] | Maximum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
7 years
|
|
Furniture and Fixtures [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 323,755
|
258,414
|
Furniture and Fixtures [Member] | Minimum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
5 years
|
|
Furniture and Fixtures [Member] | Maximum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
10 years
|
|
Leasehold Improvements [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 107,983
|
19,631
|
Leasehold Improvements [Member] | Minimum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
2 years
|
|
Leasehold Improvements [Member] | Maximum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Useful life |
5 years
|
|
Internal Use Software [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Property and equipment, gross |
$ 1,618,998
|
$ 1,618,998
|
Useful life |
5 years
|
|
X |
- DefinitionAmount of accumulated depreciation, depletion and amortization for physical assets used in the normal conduct of business to produce goods and services.
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v3.23.3
SCHEDULE OF CHANGES IN FAIR VALUE FOR CONTINGENT EARNOUT CONSIDERATION (Details)
|
9 Months Ended |
Sep. 30, 2023
USD ($)
|
Accounting Policies [Abstract] |
|
Balance at December 31, 2022 |
$ 7,166,691
|
Additions |
893,000
|
Changes in fair value of earnout liabilities |
(1,494,910)
|
Settlements |
(692,795)
|
Balance at September 30, 2023 |
$ 5,871,986
|
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v3.23.3
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Details Narrative) - USD ($)
|
3 Months Ended |
9 Months Ended |
|
Sep. 30, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Dec. 31, 2022 |
Property, Plant and Equipment [Line Items] |
|
|
|
|
|
Proceeds from royalties |
|
|
$ 50,250
|
|
|
Bad debt expense |
$ 128,061
|
$ 25,000
|
214,061
|
$ 220,000
|
|
Allowance for doubtful accounts |
511,089
|
|
511,089
|
|
$ 265,089
|
Accounts receivable allowances |
5,297
|
|
5,297
|
|
4,761
|
Inventory obsolescence expense |
152,701
|
129,689
|
222,691
|
289,406
|
|
Allowance for obsolete and slow-moving inventory |
327,492
|
|
327,492
|
|
$ 523,832
|
Depreciation |
$ 116,596
|
$ 106,347
|
332,762
|
$ 300,655
|
|
Minimum [Member] |
|
|
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
|
|
Proceeds from royalties |
|
|
201,000
|
|
|
BioStructures LLC [Member] |
|
|
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
|
|
Proceeds from royalties |
|
|
$ 50,250
|
|
|
Royalty percentage |
|
|
2.00%
|
|
|
BioStructures LLC [Member] | Minimum [Member] |
|
|
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
|
|
Proceeds from royalties |
|
|
$ 201,000
|
|
|
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v3.23.3
SCHEDULE OF PURCHASE CONSIDERATIONS (Details) - USD ($)
|
|
1 Months Ended |
Apr. 04, 2022 |
Jul. 31, 2022 |
Precision Healing Inc [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Cash paid to non-accredited investors |
$ 125,370
|
|
Cash paid for fractional shares |
596
|
|
Carrying value of equity method investment in Precision Healing |
1,803,440
|
|
Fair value of contingent earnout consideration |
3,882,151
|
|
Direct transaction costs |
1,061,137
|
|
Total purchase consideration |
$ 16,581,783
|
|
Precision Healing Inc [Member] | Equity Option [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Equity Shares |
144,191
|
|
Fair value of stok issued, value |
$ 4,109,750
|
|
Precision Healing Inc [Member] | Common Stock [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Equity Shares |
165,738
|
|
Fair value of stok issued, value |
$ 5,096,444
|
|
Precision Healing Inc [Member] | Warrant [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Equity Shares |
16,725
|
|
Fair value of stok issued, value |
$ 502,895
|
|
Scendia Purchase Agreement [Member] | Common Stock [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Equity Shares |
|
291,686
|
Fair value of stok issued, value |
|
$ 6,032,066
|
Fair value of contingent earnout consideration |
|
3,000,000
|
Total purchase consideration |
|
10,594,734
|
Cash consideration |
|
$ 1,562,668
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v3.23.3
SCHEDULE OF PURCHASE CONSIDERATION ON FAIR VALUE OF ASSETS ACQUIRED (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Restructuring Cost and Reserve [Line Items] |
|
|
Goodwill |
$ 3,601,781
|
$ 3,601,781
|
Precision Healing Inc [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Cash |
32,202
|
|
Net working capital (excluding cash) |
(308,049)
|
|
Fixed assets, net |
9,228
|
|
Deferred tax assets |
278,661
|
|
Intellectual property |
20,325,469
|
|
Assembled workforce |
664,839
|
|
Deferred tax liabilities |
(4,420,567)
|
|
Net assets acquired |
16,581,783
|
|
Scendia Purchase Agreement [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Cash |
201,406
|
|
Net working capital (excluding cash) |
1,294,499
|
|
Noncontrolling interest in Sanara Biologics, LLC |
2,638
|
|
Customer relationships |
7,155,000
|
|
Fixed assets, net |
42,300
|
|
Deferred tax liabilities |
(1,702,890)
|
|
Goodwill |
3,601,781
|
|
Net assets acquired |
10,594,734
|
|
Applied Asset Purchase [Member] |
|
|
Restructuring Cost and Reserve [Line Items] |
|
|
Inventory |
30,007
|
|
Equipment |
33,062
|
|
Intellectual property |
16,728,968
|
|
Net assets acquired |
$ 16,792,037
|
|
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v3.23.3
PRECISION HEALING MERGER (Details Narrative) - USD ($)
|
|
|
1 Months Ended |
9 Months Ended |
Apr. 01, 2023 |
Apr. 04, 2022 |
Apr. 30, 2022 |
Sep. 30, 2023 |
Asset Acquisition [Line Items] |
|
|
|
|
Merger agreement cash consideration |
$ 16,792,037
|
|
|
|
Transaction expenses |
162,743
|
|
|
|
Number of stock options exercised |
|
|
|
50,318
|
Warrants to purchase common stock |
|
|
4,424
|
|
Warrant initial exercise price |
|
|
$ 7.32
|
|
Expiration date |
|
|
Apr. 22, 2031
|
|
Payments to contingent consideration |
$ 893,000
|
|
|
|
Precision Healing Inc [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Share price |
|
$ 30.75
|
|
|
Precision Healing Inc [Member] | Warrants One [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Warrants to purchase common stock |
|
4,424
|
|
|
Warrant initial exercise price |
|
$ 7.32
|
|
|
Expiration date |
|
Apr. 22, 2031
|
|
|
Precision Healing Inc [Member] | Warrants Two [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Warrants to purchase common stock |
|
12,301
|
|
|
Warrant initial exercise price |
|
$ 12.05
|
|
|
Expiration date |
|
Aug. 10, 2030
|
|
|
Precision Healing Inc [Member] | Precision Healing Plan [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Number of stock options exercised |
|
144,191
|
|
|
Weighted exercise price |
|
$ 10.71
|
|
|
Accredited Investors [Member] | Precision Healing Inc [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Number of shares issued, acquisitions, value |
|
165,738
|
|
|
Precision Healing Inc [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Merger agreement cash consideration |
|
|
$ 125,966
|
|
Transaction expenses |
|
$ 600,000
|
|
|
Payments to contingent consideration |
|
|
$ 10,000,000.0
|
|
Precision Healing Inc [Member] | Stockholders [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Merger agreement cash consideration |
|
125,966
|
|
|
Precision Healing Inc [Member] | Security Holders [Member] |
|
|
|
|
Asset Acquisition [Line Items] |
|
|
|
|
Payments to contingent consideration |
|
$ 10,000,000.0
|
|
|
Common stock conversion price |
|
$ 27.13
|
|
|
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v3.23.3
SCENDIA PURCHASE AGREEMENT (Details Narrative) - USD ($)
|
|
1 Months Ended |
12 Months Ended |
Apr. 01, 2023 |
Aug. 31, 2023 |
Jul. 31, 2022 |
Dec. 31, 2022 |
Merger agreement cash consideration |
$ 16,792,037
|
|
|
|
Cash consideration |
|
|
$ 10,000,000.0
|
|
Number of shares |
|
|
486,145
|
|
Earnout payment |
|
$ 693,000
|
|
|
Scendia Acquisition [Member] |
|
|
|
|
Acquisition costs |
|
|
|
$ 187,000
|
Purchase Agreement [Member] |
|
|
|
|
Issuance of common stock for purchase of assets |
|
|
291,686
|
|
Number of shares issued |
|
|
94,798
|
|
Proceeds from offering |
|
|
$ 1,950,000
|
|
Purchase Agreement [Member] | Scendia Biologics LLC [Member] |
|
|
|
|
Merger agreement cash consideration |
|
|
$ 1,600,000
|
|
Scendia Biologics LLC [Member] |
|
|
|
|
Equity method ownership percentage |
|
|
50.00%
|
|
Membership Interest Purchase Agreement [Member] |
|
|
|
|
Equity method ownership percentage |
|
|
100.00%
|
|
Scendia Biologics LLC [Member] | Scendia Purchase Agreement [Member] |
|
|
|
|
Equity method ownership percentage |
|
|
100.00%
|
|
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v3.23.3
SCHEDULE OF PURCHASE CONSIDERATION (Details)
|
Apr. 01, 2023
USD ($)
shares
|
Applied Asset Purchase |
|
Cash Closing Consideration |
$ 9,750,000
|
Fair value of Stock Closing Consideration |
$ 3,089,645
|
Equity Shares | shares |
73,809
|
Fair value of Installment Payments |
$ 2,040,808
|
Cash paid for inventory |
30,007
|
Fair value of Petito Services Agreement defined payments |
825,834
|
Fair value of Petito Services Agreement contingent consideration |
893,000
|
Direct transaction costs |
162,743
|
Total purchase consideration |
$ 16,792,037
|
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v3.23.3
APPLIED ASSET PURCHASE (Details Narrative) $ in Thousands |
Aug. 01, 2023
USD ($)
shares
|
Business Acquisition, Contingent Consideration [Line Items] |
|
Cash consideration |
$ 10,000
|
Applied Asset Purchase [Member] |
|
Business Acquisition, Contingent Consideration [Line Items] |
|
Purchase agreement description |
As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of
$12,000 per month during the term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual
collections from net sales of certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment
equal to five percent (5%) for the first $50.0 million in aggregate collections from net sales of certain future products and a royalty
payment of two and one-half percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding
$50.0 million but up to $100.0 million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted
by the Company and (v) $1.0 million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect
to the incentive payments described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
|
Cash Closing Consideration [Member] |
|
Business Acquisition, Contingent Consideration [Line Items] |
|
Payments to acquire productive assets |
$ 15,250
|
Cash consideration |
$ 9,750
|
Stock issued during period shares issued for services | shares |
73,809
|
Stock Closing Consideration [Member] |
|
Business Acquisition, Contingent Consideration [Line Items] |
|
Payments to acquire productive assets |
$ 3,000
|
Cash consideration |
$ 2,500
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v3.23.3
SCHEDULE OF FINITE LIVED INTANGIBLE ASSETS (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Finite-Lived Intangible Assets [Line Items] |
|
|
Net |
$ 45,991,466
|
$ 31,509,980
|
Licensing Agreements [Member] |
|
|
Finite-Lived Intangible Assets [Line Items] |
|
|
Cost |
4,793,879
|
4,793,879
|
Accumulated amortization |
(1,246,115)
|
(980,583)
|
Net |
3,547,764
|
3,813,296
|
Patents [Member] |
|
|
Finite-Lived Intangible Assets [Line Items] |
|
|
Cost |
38,664,548
|
21,935,580
|
Accumulated amortization |
(2,598,220)
|
(1,492,057)
|
Net |
36,066,328
|
20,443,523
|
Customer Relationships and Other [Member] |
|
|
Finite-Lived Intangible Assets [Line Items] |
|
|
Cost |
7,947,332
|
7,947,332
|
Accumulated amortization |
(1,569,958)
|
(694,171)
|
Net |
6,377,374
|
7,253,161
|
Amortizable Intangible Assets [Member] |
|
|
Finite-Lived Intangible Assets [Line Items] |
|
|
Cost |
51,405,759
|
34,676,791
|
Accumulated amortization |
(5,414,293)
|
(3,166,811)
|
Net |
$ 45,991,466
|
$ 31,509,980
|
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v3.23.3
SCHEDULE OF FUTURE AMORTIZATION EXPENSE (Details)
|
Sep. 30, 2023
USD ($)
|
Goodwill and Intangible Assets Disclosure [Abstract] |
|
Remainder of 2023 |
$ 974,018
|
2024 |
3,896,070
|
2025 |
3,896,070
|
2026 |
3,878,815
|
2027 |
3,764,962
|
2028 |
3,731,721
|
Thereafter |
25,849,810
|
Total |
$ 45,991,466
|
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v3.23.3
INTANGIBLE ASSETS (Details Narrative) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
|
|
|
Weighted average useful life |
|
|
14 years 6 months
|
|
Amortization of intangible assets |
$ 881,079
|
$ 708,534
|
$ 2,247,482
|
$ 1,256,097
|
X |
- DefinitionWeighted average amortization period of finite-lived intangible assets acquired either individually or as part of a group of assets, in 'PnYnMnDTnHnMnS' format, for example, 'P1Y5M13D' represents the reported fact of one year, five months, and thirteen days.
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v3.23.3
SCHEDULE OF INVESTMENTS (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Cost method investment |
$ 3,084,278
|
$ 3,084,278
|
Total Investments |
3,084,278
|
3,084,278
|
Precision Healing Inc [Member] |
|
|
Equity method investment |
|
|
Economic interest |
|
|
Direct Dermatology Inc. [Member] |
|
|
Cost method investment |
$ 1,000,000
|
$ 1,000,000
|
Pixalere Healthcare Inc. [Member] |
|
|
Cost method investment |
$ 2,084,278
|
$ 2,084,278
|
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v3.23.3
INVESTMENTS IN EQUITY SECURITIES (Details Narrative) - USD ($)
|
1 Months Ended |
3 Months Ended |
9 Months Ended |
12 Months Ended |
|
Mar. 31, 2022 |
Dec. 31, 2021 |
Oct. 31, 2021 |
Jun. 30, 2021 |
Feb. 28, 2021 |
Nov. 30, 2020 |
Jul. 31, 2020 |
Sep. 30, 2023 |
Mar. 31, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Dec. 31, 2021 |
Dec. 31, 2022 |
Long term investments |
|
|
|
|
|
|
|
$ 3,084,278
|
|
|
$ 3,084,278
|
|
|
$ 3,084,278
|
Value of shares purchased |
|
|
|
|
|
|
|
|
$ 1,033,761
|
|
|
|
|
|
Investments |
|
|
|
|
|
|
|
3,084,278
|
|
|
3,084,278
|
|
|
$ 3,084,278
|
Loss on equity method investment |
|
|
|
|
|
|
|
|
|
|
|
$ 379,633
|
|
|
Precision Healing Inc [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss on equity method investment |
|
|
|
|
|
|
|
|
|
|
|
$ 379,633
|
|
|
Series B-2 Preferred Shares [Member] | Direct Derm's [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Ownership interest |
|
|
|
|
|
|
2.90%
|
8.10%
|
|
|
8.10%
|
|
|
|
Series A Convertible Preferred Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Ownership interest |
|
|
|
|
|
12.60%
|
|
|
|
|
|
|
|
|
Series A Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Ownership interest |
|
|
|
29.00%
|
22.40%
|
|
|
|
|
|
|
|
|
|
Series B-2 Preferred Shares [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Long term investments |
|
|
|
|
|
|
$ 500,000
|
|
|
|
|
|
|
|
Purchase of additional shares |
|
|
|
|
|
|
7,142,857
|
|
|
|
|
|
|
|
Series B-2 Preferred Shares [Member] | Direct Derm's [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Purchase of additional shares |
3,571,429
|
|
|
|
|
|
|
|
|
|
|
|
3,571,430
|
|
Value of shares purchased |
$ 250,000
|
|
|
|
|
|
|
|
|
|
|
|
$ 250,000
|
|
Series A Convertible Preferred Stock [Member] | Precision Healing Inc [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Purchase of additional shares |
|
|
|
|
|
150,000
|
|
|
|
|
|
|
|
|
Value of shares purchased |
|
|
|
|
|
$ 600,000
|
|
|
|
|
|
|
|
|
Conversion of stock |
|
|
|
|
|
150,000
|
|
|
|
|
|
|
|
|
Series A Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Purchase of additional shares |
|
150,000
|
125,000
|
125,000
|
150,000
|
|
|
|
|
|
|
|
|
|
Value of shares purchased |
|
$ 600,000
|
$ 500,000
|
|
|
|
|
|
|
|
|
|
|
|
Investments |
|
|
|
$ 500,000
|
$ 600,000
|
|
|
|
|
|
|
|
|
|
Series A Stock [Member] | Precision Healing Inc [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Conversion of stock |
|
|
|
|
150,000
|
|
|
|
|
|
|
|
|
|
Class A Preferred Shares [Member] | Pixalere Healthcare Inc. [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Purchase of additional shares |
|
|
|
278,587
|
|
|
|
|
|
|
|
|
|
|
Investments |
|
|
|
$ 2,084,278
|
|
|
|
|
|
|
|
|
|
|
Conversion of shares |
|
|
|
27.30%
|
|
|
|
|
|
|
|
|
|
|
Class A Preferred Shares [Member] | Pixalere Healthcare Inc. [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Ownership interest |
|
|
|
27.30%
|
|
|
|
|
|
|
|
|
|
|
Ownership amount |
|
|
|
$ 93,879
|
|
|
|
|
|
|
|
|
|
|
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v3.23.3
SCHEDULE OF OPERATING LEASE LIABILITY (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Operating Leases |
|
|
Remainder of 2023 |
$ 116,285
|
|
2024 |
505,017
|
|
2025 |
532,053
|
|
2026 |
379,529
|
|
2027 |
297,947
|
|
2028 |
295,689
|
|
Thereafter |
604,049
|
|
Total lease payments |
2,730,569
|
|
Less imputed interest |
(562,070)
|
|
Present Value of Lease Liabilities |
2,168,499
|
|
Operating lease liabilities – current |
322,206
|
$ 313,933
|
Operating lease liabilities – long-term |
$ 1,846,293
|
$ 505,291
|
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v3.23.3
OPERATING LEASES (Details Narrative) - USD ($)
|
9 Months Ended |
|
Sep. 30, 2023 |
Sep. 30, 2022 |
Dec. 31, 2022 |
Property, Plant and Equipment [Line Items] |
|
|
|
Operating lease right of use asset |
$ 2,094,188
|
|
$ 806,402
|
Operating lease liability |
2,168,499
|
|
|
Operating lease expenses |
295,268
|
$ 210,317
|
|
Operating lease payments |
$ 264,291
|
$ 210,897
|
|
Weighted average remaining lease term |
6 years
|
|
|
Weighted average discount rate |
7.59%
|
|
|
Office Space One [Member] |
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
Remaining lease term |
87 months
|
|
|
Office Space Two [Member] |
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
Remaining lease term |
40 months
|
|
|
Office Space Three [Member] |
|
|
|
Property, Plant and Equipment [Line Items] |
|
|
|
Remaining lease term |
23 months
|
|
|
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v3.23.3
SCHEDULE OF LONG-TERM DEBT (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Short-Term Debt [Line Items] |
|
|
Total debt |
$ 9,750,000
|
|
Less: debt issuance costs, net of accumulated amortization of $2,055 and zero |
(59,603)
|
|
Long-term debt |
9,690,397
|
|
Less: current portion of debt |
232,143
|
|
Long-term debt, net of current portion |
9,458,254
|
|
Term Loan [Member] |
|
|
Short-Term Debt [Line Items] |
|
|
Total debt |
$ 9,750,000
|
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v3.23.3
SCHEDULE OF MATURITIES OUTSTANDING DEBT (Details) - USD ($)
|
Sep. 30, 2023 |
Dec. 31, 2022 |
Debt And Credit Facilities |
|
|
Remainder of 2023 |
|
|
2024 |
580,357
|
|
2025 |
1,625,000
|
|
2026 |
1,950,000
|
|
2027 |
1,950,000
|
|
2028 |
3,644,643
|
|
Thereafter |
|
|
Total debt |
$ 9,750,000
|
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v3.23.3
DEBT AND CREDIT FACILITIES (Details Narrative) - USD ($)
|
3 Months Ended |
9 Months Ended |
|
|
|
|
Sep. 30, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Aug. 05, 2024 |
Aug. 11, 2023 |
Aug. 01, 2023 |
Dec. 31, 2022 |
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
|
|
|
|
|
Unamortized debt issuance costs |
$ 59,603
|
|
$ 59,603
|
|
|
|
|
$ 0
|
Debt issuance costs |
$ 2,055
|
$ 0
|
$ 2,055
|
$ (0)
|
|
|
|
|
Term Loan [Member] |
|
|
|
|
|
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
|
|
|
|
|
Term loan percentage |
8.30%
|
|
8.30%
|
|
|
|
|
|
Debt issuance costs |
$ 61,658
|
|
|
|
|
|
|
|
Loan Agreement [Member] |
|
|
|
|
|
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
|
|
|
|
|
Principal amount |
|
|
|
|
|
$ 12,000,000.0
|
|
|
Loan agreement percentage |
|
|
|
|
|
|
100.00%
|
|
Loan bank advance |
|
|
|
|
|
$ 9,750,000
|
|
|
Bank, interest rate |
|
|
|
|
3.00%
|
|
|
|
Loan agreement, description |
|
|
(i) create, assume or guarantee certain liabilities, (ii) create, assume or suffer
liens securing indebtedness, (iii) make or permit loans and advances, (iv) acquire any assets outside the ordinary course of business,
(v) consolidate, merge or sell all or a material part of its assets, (vi) pay dividends or other distributions on, or redeem or repurchase,
interest in an obligor, including the Company, as guarantor (vii) cease, suspend or materially curtail business operations or (viii)
engage in certain affiliate transactions. In addition, the Loan Agreement contains financial covenants that require SMAT to maintain
(i) a minimum Debt Services Coverage Ratio of 1.2 to 1.0 as of the last day of each applicable fiscal quarter and (ii) a maximum Cash
Flow Leverage Ratio of not more than (a) 4.5 to 1.0 as of the last day of the fiscal quarter ending on September 30, 2023, (b) 4.0 to
1.0 as of the last day of each fiscal quarter ending on December 31, 2023 and March 31, 2024, (c) 3.5 to 1.0 as of the last day of each
fiscal quarter ending June 30, 2024 and September 30, 2024 and (d) 3.0 to 1.0 as of the last day of each fiscal quarter thereafter.
|
|
|
|
|
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- DefinitionAmount of accumulated amortization of debt issuance costs classified as noncurrent.
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v3.23.3
COMMITMENTS AND CONTINGENCIES (Details Narrative) - USD ($)
|
|
|
|
|
1 Months Ended |
3 Months Ended |
9 Months Ended |
12 Months Ended |
|
|
Aug. 01, 2023 |
Apr. 01, 2023 |
Jul. 07, 2019 |
Aug. 27, 2018 |
Dec. 31, 2022 |
Jul. 31, 2022 |
Apr. 30, 2022 |
May 31, 2020 |
Apr. 30, 2020 |
Oct. 31, 2019 |
May 31, 2019 |
Sep. 30, 2023 |
Mar. 31, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Dec. 31, 2022 |
Aug. 31, 2023 |
Apr. 04, 2022 |
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payment of cash |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$ 9,942,750
|
$ 2,191,919
|
|
|
|
Proceeds from royalties received |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
50,250
|
|
|
|
|
Annual royalty obligation |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$ 4,020
|
|
|
|
|
Cash consideration |
|
$ 16,792,037
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Options to acquire shares |
|
|
|
|
|
|
144,191
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted exercise price |
|
|
|
|
|
|
$ 10.71
|
|
|
|
|
|
|
|
|
|
|
|
|
Warrants to purchase shares |
|
|
|
|
|
|
4,424
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercise price |
|
|
|
|
|
|
$ 7.32
|
|
|
|
|
|
|
|
|
|
|
|
|
Expiration date |
|
|
|
|
|
|
Apr. 22, 2031
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments receive |
|
$ 893,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
cash |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$ 693,000
|
|
Cash consideration |
|
|
|
|
|
$ 10,000,000.0
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Number of shares |
|
|
|
|
|
486,145
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income |
|
|
|
|
|
|
|
|
|
|
|
$ (34,579)
|
|
$ (58,792)
|
$ (111,455)
|
(98,485)
|
|
|
|
Cash Closing Consideration [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments to Acquire Productive Assets |
$ 15,250,000
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Warrants to purchase shares |
|
|
|
|
|
|
12,301
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercise price |
|
|
|
|
|
|
$ 12.05
|
|
|
|
|
|
|
|
|
|
|
|
|
Expiration date |
|
|
|
|
|
|
Aug. 10, 2030
|
|
|
|
|
|
|
|
|
|
|
|
|
Number of shares isssued |
|
|
|
|
|
|
|
|
|
|
|
|
26,143
|
|
|
|
|
|
|
Precision Healing Inc [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash consideration |
|
|
|
|
|
|
$ 125,966
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments receive |
|
|
|
|
|
|
$ 10,000,000.0
|
|
|
|
|
|
|
|
|
|
|
|
|
Precision Healing [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments receive |
|
|
|
|
|
|
|
|
$ 10,000,000.0
|
|
|
|
|
|
|
|
|
|
|
2009 [Member] | Resorbable Bone Hemostat [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Royalty percentage |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
2.00%
|
|
|
|
|
Rochal [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payment of cash |
|
|
|
|
|
|
|
$ 500,000
|
|
|
|
|
|
|
|
|
|
|
|
Accredited Investors [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of shares |
|
|
|
|
|
|
165,738
|
|
|
|
|
|
|
|
|
|
|
|
|
Nonaccredited Investors [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Share price |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$ 30.75
|
Minimum [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Proceeds from royalties received |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$ 201,000
|
|
|
|
|
Minimum [Member] | 2009 [Member] | Resorbable Bone Hemostat [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments for royalties |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
201,000
|
|
|
|
|
Precision Healing [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Payment in cash |
|
|
|
|
|
|
$ 600,000
|
|
|
|
|
|
|
|
|
|
|
|
|
Share price |
|
|
|
|
|
|
$ 27.13
|
|
$ 27.13
|
|
|
|
|
|
|
|
|
|
|
Wound Care Solutions Limited [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income |
|
|
|
|
$ 242,000
|
|
$ 220,000
|
|
|
|
$ 200,000
|
|
|
|
|
|
|
|
|
Wound Care Solutions Limited [Member] | 2021 Through 2024 [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income, percentage |
|
|
|
|
|
|
|
|
|
|
10.00%
|
|
|
|
|
|
|
|
|
Cost of Sales [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Royalty expense |
|
|
|
|
|
|
|
|
|
|
|
9,209
|
|
432,809
|
1,060,035
|
1,245,775
|
|
|
|
Annual royalty obligation |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
16,080
|
|
|
|
|
Sub License Agreement [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss Contingencies [Line Items] |
|
|
|
|
|
|
|
|
|
|
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License agreement and royalties description |
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In
August 2018, the Company entered into the Sublicense Agreement with CGI Cellerate RX to distribute CellerateRX Surgical and HYCOL
products into the surgical and wound care markets. Pursuant to the Sublicense Agreement, the Company pays royalties of 3-5% of
annual collected net sales of CellerateRX Surgical and HYCOL. As amended in January 2021, the term of the sublicense extends through
May 2050, with automatic successive year-to-year renewal terms thereafter so long as the Company’s Net Sales (as defined in
the Sublicense Agreement) each year are equal to or in excess of $1,000,000. If the Company’s Net Sales fall below $1,000,000
for any year after the initial expiration date, CGI Cellerate RX will have the right to terminate the Sublicense Agreement upon
written notice.
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BIAKOS License Agreement [Member] |
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Loss Contingencies [Line Items] |
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Royalty expense |
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$ 32,499
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$ 30,000
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97,499
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$ 90,000
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BIAKOS License Agreement [Member] | Rochal Industries LLC [Member] |
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Loss Contingencies [Line Items] |
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Increase of royalties payable |
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10,000
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BIAKOS License Agreement [Member] | Rochal Industries LLC [Member] | Minimum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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2.00%
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Payments for royalties |
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$ 120,000
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BIAKOS License Agreement [Member] | Rochal Industries LLC [Member] | Maximum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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4.00%
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Payments for royalties |
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150,000
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BIAKOS Agreement [Member] | Maximum [Member] |
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Loss Contingencies [Line Items] |
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Payment for additional royalties |
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$ 1,000,000
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ABF License Agreement [Member] |
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Loss Contingencies [Line Items] |
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Royalty annual minimum percentage |
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10.00%
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ABF License Agreement [Member] | Minimum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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2.00%
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ABF License Agreement [Member] | Maximum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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4.00%
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Payments for royalties |
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$ 75,000
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Payment for additional royalties |
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$ 500,000
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Debrider License Agreement [Member] |
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Loss Contingencies [Line Items] |
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Royalty annual minimum percentage |
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10.00%
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Payment of cash |
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$ 1,000,000
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Debrider License Agreement [Member] | Minimum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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2.00%
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Payments for royalties |
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$ 100,000
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Debrider License Agreement [Member] | Maximum [Member] |
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Loss Contingencies [Line Items] |
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Royalty percentage |
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4.00%
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Payments for royalties |
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$ 150,000
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Payment for additional royalties |
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$ 1,000,000
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Royalty Agreement [Member] | 2009 [Member] | Resorbable Bone Hemostat [Member] |
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Loss Contingencies [Line Items] |
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Royalty annual minimum percentage |
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8.00%
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Purchase Agreement [Member] |
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Loss Contingencies [Line Items] |
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Acquisition consideration transferred |
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$ 7,600,000
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cash |
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$ 1,600,000
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Issuance of common stock for purchase of assets |
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291,686
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Number of shares isssued |
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94,798
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Payments to Acquire Productive Assets |
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$ 7,600,000
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Services Agreement [Member] |
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Loss Contingencies [Line Items] |
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Purchase agreement description |
As consideration for the Petito Services, the Owner is entitled to receive: (i) a base salary of $12,000 per month during the
term of the Petito Services Agreement, (ii) a royalty payment equal to three percent (3%) of the actual collections from net sales of
certain products the Owner develops or co-develops that reach commercialization, (iii) a royalty payment equal to five percent (5%) for
the first $50.0 million in aggregate collections from net sales of certain future products and a royalty payment of two and one-half
percent (2.5%) on aggregate collections from net sales of certain future products on any amounts exceeding $50.0 million but up to $100.0
million, (iv) $500,000 in cash in the event that 510(k) clearance is issued for any future product accepted by the Company and (v) $1.0
million in cash in the event that a U.S. patent is issued for a certain product; provided that with respect to the incentive payments
described in (iv) and (v) of the foregoing, the Owner shall not earn more than $2.5 million.
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v3.23.3
SUMMARY OF RESTRICTED STOCK ACTIVITY (Details)
|
9 Months Ended |
Sep. 30, 2023
$ / shares
shares
|
Equity [Abstract] |
|
Non-vested shares, beginning | shares |
181,102
|
Weighted average grant date fair value, beginning | $ / shares |
$ 22.89
|
Granted | shares |
118,912
|
Weighted average grant date fair value, granted | $ / shares |
$ 39.14
|
Vested | shares |
(129,342)
|
Weighted average grant date fair value, vested | $ / shares |
$ 22.84
|
Forfeited | shares |
(11,115)
|
Weighted average grant date fair value, forfeited | $ / shares |
$ 32.96
|
Non-vested shares, ending | shares |
159,557
|
Weighted average grant date fair value, ending | $ / shares |
$ 34.27
|
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v3.23.3
SCHEDULE OF STOCK OPTION ACTIVITY (Details) - $ / shares
|
1 Months Ended |
9 Months Ended |
Apr. 30, 2022 |
Sep. 30, 2023 |
Equity [Abstract] |
|
|
Number of options outstanding, beginning |
|
146,191
|
Weighted average exercise price outstanding, beginning |
|
$ 10.65
|
Granted |
144,191
|
|
Weighted average exercise price, Granted |
|
|
Exercised |
|
(50,318)
|
Weighted average exercise price, Exercised |
|
$ 11.58
|
Forfeited |
|
|
Weighted average exercise price, Forfeited |
|
|
Expired |
|
|
Weighted average exercise price, Expired |
|
|
Number of options outstanding, ending |
|
95,873
|
Weighted average exercise price outstanding, ending |
|
$ 10.16
|
Weighted average remaining contract life outstanding |
|
7 years 1 month 6 days
|
Number of options exercisable, ending |
|
95,873
|
Weighted average exercise price exercisable, ending |
|
$ 10.16
|
Weighted average remaining contract life exercisable, ending |
|
7 years 1 month 6 days
|
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v3.23.3
SCHEDULE OF WARRANTS TO PURCHASE COMMON STOCK (Details)
|
9 Months Ended |
Sep. 30, 2023
$ / shares
shares
|
Equity [Abstract] |
|
Number of warrants outstanding, beginning | shares |
16,725
|
Weighted average exercise price outstanding, beginning | $ / shares |
$ 10.80
|
Number of warrants, granted | shares |
|
Weighted average exercise price, granted | $ / shares |
|
Number of warrants, exercised | shares |
|
Weighted average exercise price, exercised | $ / shares |
|
Number of warrants, forfeited | shares |
|
Weighted average exercise price, forfeited | $ / shares |
|
Number of warrants, expired | shares |
|
Weighted average exercise price, expired | $ / shares |
|
Number of warrants outstanding, ending | shares |
16,725
|
Weighted average exercise price outstanding, ending | $ / shares |
$ 10.80
|
Weighted average remaining contract life outstanding |
7 years
|
Number of warrants exercisable, ending | shares |
16,725
|
Weighted average exercise price, exercisable, ending | $ / shares |
$ 10.80
|
Weighted average remaining contract life exercisable, ending |
7 years
|
X |
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v3.23.3
SHAREHOLDERS’ EQUITY (Details Narrative) - USD ($)
|
|
|
1 Months Ended |
3 Months Ended |
9 Months Ended |
|
|
Aug. 01, 2023 |
Apr. 01, 2023 |
Aug. 31, 2023 |
Feb. 28, 2023 |
Jul. 31, 2022 |
Apr. 30, 2022 |
Sep. 30, 2023 |
Mar. 31, 2023 |
Sep. 30, 2022 |
Sep. 30, 2023 |
Sep. 30, 2022 |
Apr. 04, 2022 |
Apr. 30, 2020 |
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash consideration |
|
$ 16,792,037
|
|
|
|
|
|
|
|
|
|
|
|
Options to acquire shares |
|
|
|
|
|
144,191
|
|
|
|
|
|
|
|
Weighted exercise price |
|
|
|
|
|
$ 10.71
|
|
|
|
|
|
|
|
Warrants to purchase shares |
|
|
|
|
|
4,424
|
|
|
|
|
|
|
|
Exercise price |
|
|
|
|
|
$ 7.32
|
|
|
|
|
|
|
|
Expiration date |
|
|
|
|
|
Apr. 22, 2031
|
|
|
|
|
|
|
|
Payments to contingent consideration |
|
$ 893,000
|
|
|
|
|
|
|
|
|
|
|
|
Cash |
|
|
$ 693,000
|
|
|
|
|
|
|
|
|
|
|
Cash consideration |
|
|
|
|
$ 10,000,000.0
|
|
|
|
|
|
|
|
|
Number of shares |
|
|
|
|
486,145
|
|
|
|
|
|
|
|
|
Earnout payment |
|
|
$ 693,000
|
|
|
|
|
|
|
|
|
|
|
Number of shares issued, value |
|
|
|
|
|
|
|
$ 1,033,761
|
|
|
|
|
|
Stock granted and issued |
|
|
|
|
|
|
|
|
|
107,797
|
|
|
|
Restricted stock award, gross |
|
|
|
|
|
|
|
|
|
$ 4,287,777
|
|
|
|
Share-based compensation |
|
|
|
|
|
|
$ 857,526
|
|
$ 683,202
|
2,582,163
|
$ 1,971,537
|
|
|
Unrecognized share-based compensation expense |
|
|
|
|
|
|
$ 3,980,624
|
|
|
$ 3,980,624
|
|
|
|
Unrecognized share-based compensation expense period for recognition |
|
|
|
|
|
|
|
|
|
1 year
|
|
|
|
Cash Closing Consideration [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Payments to acquire assets |
$ 15,250,000
|
|
|
|
|
|
|
|
|
|
|
|
|
Purchase Agreement [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock in equity offering, shares |
|
|
|
|
94,798
|
|
|
|
|
|
|
|
|
Payments to acquire assets |
|
|
|
|
$ 7,600,000
|
|
|
|
|
|
|
|
|
Cash |
|
|
|
|
$ 1,600,000
|
|
|
|
|
|
|
|
|
Issuance of common stock for purchase of assets |
|
|
|
|
291,686
|
|
|
|
|
|
|
|
|
Net proceeds |
|
|
|
|
$ 1,950,000
|
|
|
|
|
|
|
|
|
Common Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock in equity offering, shares |
|
|
|
|
|
|
|
26,143
|
|
|
|
|
|
Warrants to purchase shares |
|
|
|
|
|
12,301
|
|
|
|
|
|
|
|
Exercise price |
|
|
|
|
|
$ 12.05
|
|
|
|
|
|
|
|
Expiration date |
|
|
|
|
|
Aug. 10, 2030
|
|
|
|
|
|
|
|
Number of shares issued, value |
|
|
|
|
|
|
|
$ 26
|
|
|
|
|
|
Common Stock [Member] | Sales Agreement [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock in equity offering, shares |
|
|
|
|
|
|
|
|
|
26,143
|
|
|
|
Number of shares issued, value |
|
|
|
|
|
|
|
|
|
$ 1,066,000
|
|
|
|
Net proceeds |
|
|
|
|
|
|
|
|
|
$ 1,034,000
|
|
|
|
Precision Healing [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Payment in cash |
|
|
|
|
|
$ 600,000
|
|
|
|
|
|
|
|
Share price |
|
|
|
|
|
$ 27.13
|
|
|
|
|
|
|
$ 27.13
|
Cantor Fitzgerald and Co [Member] | Sales Agreement [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Percentage of commissions payable to sales agent |
|
|
|
3.00%
|
|
|
|
|
|
|
|
|
|
Cantor Fitzgerald and Co [Member] | Sales Agreement [Member] | Maximum [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Sale of stock, consideration received on transaction |
|
|
|
$ 75,000,000
|
|
|
|
|
|
|
|
|
|
Accredited Investors [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accredited investors shares |
|
|
|
|
|
165,738
|
|
|
|
|
|
|
|
Nonaccredited Investors [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Share price |
|
|
|
|
|
|
|
|
|
|
|
$ 30.75
|
|
Precision Healing Inc [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash consideration |
|
|
|
|
|
$ 125,966
|
|
|
|
|
|
|
|
Payments to contingent consideration |
|
|
|
|
|
$ 10,000,000.0
|
|
|
|
|
|
|
|
Restated 2014 Omnibus Long Term Incentive Plan [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Number of shares available for issuance |
|
|
|
|
|
|
1,412,535
|
|
|
1,412,535
|
|
|
|
Restated 2014 Omnibus Long Term Incentive Plan [Member] | Directors Officers Employees [Member] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Accumulated Other Comprehensive Income (Loss) [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock in equity offering, shares |
|
|
|
|
|
|
|
|
|
587,465
|
|
|
|
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v3.23.3
v3.23.3
RELATED PARTIES (Details Narrative) - USD ($)
|
1 Months Ended |
3 Months Ended |
9 Months Ended |
Jul. 31, 2021 |
Jan. 31, 2021 |
Sep. 30, 2023 |
Sep. 30, 2023 |
Consulting Agreement [Member] | Ms Salamone [Member] |
|
|
|
|
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] |
|
|
|
|
Professional fees |
$ 177,697
|
|
|
|
Cellerate Rx Sub License Agreement [Member] |
|
|
|
|
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] |
|
|
|
|
Net sale |
|
$ 1,000,000
|
|
|
License agreement and royalties description |
|
The Company pays royalties based on the annual Net Sales of licensed products (as defined
in the Sublicense Agreement) consisting of 3% of all collected Net Sales each year up to $12,000,000, 4% of all collected Net Sales each
year that exceed $12,000,000 up to $20,000,000, and 5% of all collected Net Sales each year that exceed $20,000,000.
|
|
|
Services Agreement [Member] |
|
|
|
|
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] |
|
|
|
|
Costs and Expenses, Related Party |
|
|
$ 44,032
|
$ 117,018
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