U.S.

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: Septemberended June 30, 2017

2021

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 No.    0-11808

WOUND MANAGEMENT TECHNOLOGIES, INC.
Number 001-39678

Texas59-2219994

SANARA MEDTECH INC.

(Exact name of Registrant as specified in its charter)

Texas

59-2219994

(State or other jurisdiction of

incorporation or organization)


(I.R.S. Employer

Identification Number)No.)

1200 Summit Ave, Suite 414, Fort Worth, Texas 76102

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 principal executive offices)

(817) 529-2300
(Registrant’s telephone number, including area code)
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 and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted 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 and post 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 acceleratedacc ;elerated filer,” “accelerated filer”, “smaller reporting company” and "emerging“emerging growth company"company” in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filer

Accelerated filer

Non-accelerated filer

(Do not check if a smaller reporting company)

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 the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes       No

As of NovemberAugust 16, 2017, 112,227,9432021, 7,626,705 shares of the Issuer's $.001Issuer’s $0.001 par value common stock were issued and 112,223,854 shares were outstanding.


WOUND MANAGEMENT TECHNOLOGIES, INC. AND SUBSIDIARIES
Form 10-Q
Quarter Ended September 30, 2017

 
Page

 

SANARA MEDTECH INC.

Form 10-Q

Quarter Ended June 30, 2021

Page

Part I – Financial Information

ITEM 1. Financial Statements

2

3

Unaudited Consolidated Balance Sheets as of SeptemberJune 30, 20172021 and December 31, 20162020

2

3

Unaudited Consolidated Statements of Operations for the Three and NineSix Months Ended SeptemberJune 30, 20172021 and 20162020

3

4

Unaudited Consolidated Statements of Changes in Shareholders’ Equity for the Three and Six Months Ended June 30, 2021 and 2020

5

Unaudited Consolidated Statements of Cash Flows for the NineSix Months Ended SeptemberJune 30, 20172021 and 20162020

4

6

Notes to Unaudited Consolidated Financial Statements

5

7

ITEM 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

12

20 

ITEM 3. Quantitative and Qualitative Disclosures about Market Risk

15

27

ITEM 4. Controls and Procedures

15

27

Part II. Other Information

ITEM 1. Legal Proceedings

15

28

ITEM 1A1A. Risk Factors

15

28

ITEM 2. Unregistered Sales of Equity Securities and Use of Proceeds

15

28

ITEM 3. Defaults upon Senior Securities

15

28

ITEM 4. Mine Safety Disclosures

15

28

ITEM 5. Other Information

15

28

ITEM 6. Exhibits

29

Signatures

30

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,” “we,” “us,” “our,” and “the Company,” refer to Sanara MedTech Inc. and its consolidated subsidiaries.

 
ITEM 6.    Exhibits162

SignaturesTable of Contents17

Part I – Financial Information

Item 1. Financial Statements

Wound Management Technologies, Inc. and Subsidiaries
Consolidated Balance Sheets
September 30, 2017 and December 31, 2016
 
 
 September 30,
 
 
 December 31,
 
 
 
2017
 
 
2016
 
Assets
 
 
 
 
 
 
Current assets
 
 
 
 
 
 
   Cash
 $151,314 
 $833,480 
   Accounts receivable, net of allowance for bad debt of $24,764 and $21,947
  814,048 
  744,044 
   Royalty receivable
  50,250 
  50,250 
   Inventory, net of allowance for obsolescence for $116,772 and $153,023
  820,908 
  348,457 
   Prepaid and other assets
  51,662 
  19,782 
Total current assets
  1,888,182 
  1,996,013 
 
    
    
Long-term assets:
    
    
   Property, plant and equipment, net of accumulated depreciation of $85,384 and $41,328
  117,336 
  34,939 
   Intangible assets, net of accumulated amortization of $408,248 and $369,974
  102,062 
  140,336 
Total long-term assets
  219,398 
  175,275 
 
    
    
Total assets
 $2,107,580 
 $2,171,288 
 
    
    
Liabilities and stockholders' deficit
    
    
 
    
    
Current liabilities
    
    
   Accounts payable
 $160,689 
 $238,229 
   Accounts payable - Related Parties
  21,842 
  93,655 
   Accrued royalties and dividends
  232,511 
  276,916 
   Accrued payable
  5,340 
  - 
   Accrued commission
  17,492 
  - 
   Deferred rent
  14,138 
  - 
   Current lease obligation
  344 
  3,766 
   Accrued interest
  460,956 
  367,411 
   Derivative liabilities
  - 
  44 
   Notes payable
  223,500 
  414,338 
   Convertible notes payable - Related parties
  1,200,000 
  - 
Total current liabilities
  2,336,812 
  1,394,359 
 
    
    
Long-term liabilities
    
    
   Convertible notes payable - Related parties
  - 
  1,200,000 
Total long-term liabilities
  - 
  1,200,000 
 
    
    
Total liabilities
  2,336,812 
  2,594,359 
 
    
    
Stockholders' deficit
    
    
   Series A Preferred Stock, $10 par value, 5,000,000 shares authorized; none issued and outstanding
  - 
  - 
   Series B Convertible Preferred Stock, $10 par value, 7,500 shares authorized; none issued and outstanding
  - 
  - 
   Series C Convertible Preferred Stock, $10 par value, 100,000 shares authorized; 85,561 issued and outstanding as of September 30, 2017 and 85,646 issued and outstanding as of December 31, 2016
  855,610 
  856,460 
   Series D Convertible Preferred Stock, $10 par value, 25,000 shares authorized; none issued and outstanding
  - 
  - 
   Series E Convertible Preferred Stock, $10 par value, 5,000 shares authorized; none issued and outstanding
  - 
  - 
   Common Stock: $.001 par value; 250,000,000 shares authorized; 112,227,943 issued and 112,223,854 outstanding as of September 30, 2017 and 109,690,387 issued and 109,686,298 outstanding as of December 31, 2016
  112,227 
  109,690 
   Additional paid-in capital
  45,931,183 
  45,822,570 
   Treasury stock
  (12,039)
  (12,039)
   Accumulated deficit
  (47,116,213)
  (47,199,752)
Total stockholders' deficit
  (229,232)
  (423,071)
 
    
    
Total liabilities and stockholders' deficit
 $2,107,580 
 $2,171,288 
 
    
    

SANARA MEDTECH INC. AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

 

 

(Unaudited)

 

 

 

 

 

June 30,

2021

 

 

December 31,

2020

 

 

 

 

 

 

 

 

Assets

Current assets

 

 

 

 

 

 

Cash

 

$24,389,004

 

 

$455,366

 

Accounts receivable, net of allowances of $138,417 and $100,189

 

 

2,445,225

 

 

 

2,217,533

 

Royalty receivable

 

 

49,344

 

 

 

49,344

 

Inventory, net of allowance for obsolescence of $295,841 and $276,603

 

 

1,538,398

 

 

 

1,148,253

 

Prepaid and other assets

 

 

497,110

 

 

 

611,817

 

Total current assets

 

 

28,919,081

 

 

 

4,482,313

 

 

 

 

 

 

 

 

 

 

Long-term assets

 

 

 

 

 

 

 

 

Property and equipment, net of accumulated depreciation of $159,732 and $124,691

 

 

1,668,994

 

 

 

678,589

 

Right of use assets – operating leases

 

 

406,024

 

 

 

467,653

 

Intangible assets, net of accumulated amortization of $983,466 and $827,108

 

 

3,785,187

 

 

 

3,097,666

 

Investment in equity securities

 

 

4,005,374

 

 

 

1,100,000

 

Total long-term assets

 

 

9,865,579

 

 

 

5,343,908

 

 

 

 

 

 

 

 

 

 

Total assets

 

$38,784,660

 

 

$9,826,221

 

 

 

 

 

 

 

 

 

 

Liabilities and shareholders’ equity

Current liabilities

 

 

 

 

 

 

 

 

Accounts payable

 

$313,569

 

 

$271,251

 

Accounts payable – related parties

 

 

57,507

 

 

 

223,589

 

Accrued royalties and expenses

 

 

527,518

 

 

 

502,191

 

Accrued bonus and commissions

 

 

2,719,258

 

 

 

2,417,277

 

Operating lease liability - current

 

 

128,301

 

 

 

125,587

 

Total current liabilities

 

 

3,746,153

 

 

 

3,539,895

 

 

 

 

 

 

 

 

 

 

Long-term liabilities

 

 

 

 

 

 

 

 

Operating lease liability – long term

 

 

290,751

 

 

 

355,797

 

Other long-term liabilities

 

 

90,293

 

 

 

90,293

 

Total long-term liabilities

 

 

381,044

 

 

 

446,090

 

 

 

 

 

 

 

 

 

 

Total liabilities

 

 

4,127,197

 

 

 

3,985,985

 

 

 

 

 

 

 

 

 

 

Shareholders’ equity

 

 

 

 

 

 

 

 

Common Stock: $0.001 par value, 20,000,000 shares authorized; 7,612,336 issued and outstanding as of June 30, 2021 and 6,297,008 issued and outstanding as of December 31, 2020

 

 

7,612

 

 

 

6,297

 

Additional paid-in capital

 

 

44,487,958

 

 

 

13,176,576

 

Accumulated deficit

 

 

(9,385,478)

 

 

(7,032,242)

Total Sanara MedTech shareholders’ equity

 

 

35,110,092

 

 

 

6,150,631

 

Equity attributable to noncontrolling interest

 

 

(452,629)

 

 

(310,395)

Total shareholders’ equity

 

 

34,657,463

 

 

 

5,840,236

 

 

 

 

 

 

 

 

 

 

Total liabilities and shareholders’ equity

 

$38,784,660

 

 

$9,826,221

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.


Wound Management Technologies, Inc. And Subsidiaries
Consolidated Statements of Operations
For the Three and Nine Months Ended September 30, 2017 and 2016
(Unaudited)
 
 
Three Months Ended
 
 
Nine Months Ended
 
 
 
September 30
 
 
September 30
 
 
 
2017
 
 
2016
 
 
2017
 
 
2016
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Revenues
 $1,549,016 
 $1,409,530 
 $4,607,162 
 $3,762,681 
 
    
    
    
    
Cost of goods sold
  230,049 
  211,639 
  568,071 
  612,514 
 
    
    
    
    
Gross profit
  1,318,967 
  1,197,891 
  4,039,091 
  3,150,167 
 
    
    
    
    
Operating expenses
    
    
    
    
  Selling, general and administrative expenses
  1,303,344 
  963,738 
  3,799,644 
  2,827,340 
  Other administrative expenses
  - 
  - 
  - 
  818,665 
  Depreciation and amortization
  41,400 
  15,282 
  82,329 
  45,601 
  Bad debt expense
  2,998 
  2,718 
  8,913 
  7,345 
Total operating expenses
  1,347,742 
  981,738 
  3,890,886 
  3,698,951 
 
    
    
    
    
Operating income / (loss)
  (28,775)
  216,153 
  148,205 
  (548,784)
 
    
    
    
    
Other income / (expense)
    
    
    
    
  Change in fair value of Derivative Liability
  6 
  118 
  44 
  205 
  Other income
  14 
  1 
  65 
  1 
  Debt forgiveness
  - 
  7,648 
  50,646 
  30,592 
  Interest expense
  (19,807)
  (42,433)
  (115,421)
  (132,689)
Total other income / (expense)
  (19,787)
  (34,666)
  (64,666)
  (101,891)
 
    
    
    
    
Net income / (loss)
  (48,562)
  181,487 
  83,539 
  (650,675)
 
    
    
    
    
Series C preferred stock dividends
  (42,873)
  (75,031)
  (100,677)
  (213,435)
 
    
    
    
    
Net income / (loss) available to common stockholders
 $(91,435)
 $106,456 
 $(17,138)
 $(864,110)
 
    
    
    
    
Basic loss per share of common stock
 $(0.00)
 $0.00 
 $(0.00)
 $(0.01)
 
    
    
    
    
Diluted loss per share of common stock
 $(0.00)
 $0.00 
 $(0.00)
 $(0.01)
 
    
    
    
    
Weighted average number of common shares outstanding basic
  111,161,335 
  108,539,909 
  110,536,584 
  108,397,112 
 
    
    
    
    
Weighted average number of common shares outstanding diluted
  111,161,335 
  194,229,681 
  110,536,584 
  108,397,112 
 
    
    
    
    

3

Table of Contents

SANARA MEDTECH INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED)

 

 

Three Months Ended

 

 

Six Months Ended

 

 

 

June 30,

 

 

June 30,

 

 

 

2021

 

 

2020

 

 

2021

 

 

2020

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net Revenue

 

$6,277,133

 

 

$2,967,183

 

 

$11,286,569

 

 

$6,491,514

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Cost of goods sold

 

 

536,405

 

 

 

348,675

 

 

 

1,010,838

 

 

 

678,863

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Gross profit

 

 

5,740,728

 

 

 

2,618,508

 

 

 

10,275,731

 

 

 

5,812,651

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Operating expenses

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Selling, general and administrative expenses

 

 

6,562,144

 

 

 

3,582,511

 

 

 

11,971,874

 

 

 

8,514,662

 

Research and development

 

 

103,981

 

 

 

41,516

 

 

 

222,193

 

 

 

45,903

 

Depreciation and amortization

 

 

100,807

 

 

 

74,221

 

 

 

191,398

 

 

 

127,726

 

Total operating expenses

 

 

6,766,932

 

 

 

3,698,248

 

 

 

12,385,465

 

 

 

8,688,291

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Operating loss

 

 

(1,026,204)

 

 

(1,079,740)

 

 

(2,109,734)

 

 

(2,875,640)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Other expense

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Other expense, related

 

 

0

 

 

 

(48,716)

 

 

0

 

 

 

(85,474)

Interest expense

 

 

0

 

 

 

(1,101)

 

 

(711)

 

 

(9,455)

Share of losses from equity method investment

 

 

(179,769)

 

 

0

 

 

 

(278,904)

 

 

0

 

Total other expense

 

 

(179,769)

 

 

(49,817)

 

 

(279,615)

 

 

(94,929)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

 

(1,205,973)

 

 

(1,129,557)

 

 

(2,389,349)

 

 

(2,970,569)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Less: Net loss attributable to noncontrolling interest

 

 

(34,481)

 

 

(3,793)

 

 

(36,113)

 

 

(7,848)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss attributable to Sanara MedTech common shareholders

 

$(1,171,492)

 

$(1,125,764)

 

$(2,353,236)

 

$(2,962,721)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss per share of common stock, basic and diluted

 

$(0.16)

 

$(0.18)

 

$(0.33)

 

$(0.54)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Weighted average number of common shares outstanding, basic and diluted

 

 

7,496,604

 

 

 

6,203,577

 

 

 

7,158,503

 

 

 

5,477,759

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.


Wound Management Technologies, Inc. and Subsidiaries
Consolidated Statements of Cash Flows
For the Nine Months Ended September 30, 2017 and 2016
(Unaudited)
 
 
Nine Months Ended
 
 
 
September 30,  
 
 
 
2017
 
 
2016
 
 
 
 
 
 
 
 
Cash flows from operating activities:
 
 
 
 
 
 
Net income (loss)
 $83,539 
 $(650,675)
Adjustments to reconcile net loss to net cash used in operating activities
    
  - 
Depreciation and amortization
  82,330 
  45,601 
Gain on forgiveness of debt
  (50,646)
  (30,592)
Bad debt expense
  8,913 
  7,345 
Common stock issued for services
  60,250 
  12,876 
(Gain) loss on change in fair value of derivative liabilities
  (44)
  (206)
(Gain) loss on issuance of debt for warrants
  - 
  758,665 
Changes in assets and liabilities:
    
    
(Increase) decrease in accounts receivable
  (78,917)
  (287,601)
(Increase) decrease in royalities receivable
  - 
  150,750 
(Increase) decrease in inventory
  (472,451)
  (167,562)
(Increase) decrease in prepaids and other assets
  (31,880)
  108,014 
Increase (decrease) in accrued royalties and dividends
  (44,405)
  (100,761)
Increase (decrease) in accounts payable
  (37,831)
  34,842 
Increase (decrease) in accounts payable related parties
  (71,813)
  387 
Increase (decrease) in accrued liabilities
  36,970 
  - 
Increase (decrease) in accrued interest payable
  104,482 
  108,826 
Net cash flows (used in) operating activities
  (411,503)
  (10,091)
 
    
    
Cash flows from investing activities:
    
    
Purchase of property and equipment
  (126,453)
  (3,029)
Net cash flows used in investing activities
  (126,453)
  (3,029)
 
    
    
Cash flows from financing activities:
    
    
Payments on capital lease obligation
  (3,422)
  (3,557)
Payments on debt
  (190,838)
  (172,700)
Cash proceeds from sale of series C preferred stock
  50,050 
  450,000 
Net cash flows provided by (used in) financing activities
  (144,210)
  273,743 
 
    
    
Net increase (decrease) in cash
  (682,166)
  260,623 
Cash and cash equivalents, beginning of period
  833,480 
  182,337 
Cash and cash equivalents, end of period
 $151,314 
 $442,960 
 
    
    
Cash paid during the period for:
    
    
Interest
 $10,937 
 $23,863 
 
    
    
Supplemental non-cash investing and financing activities:
    
    
Common stock issued for Series C dividends
  137 
  99 
Common stock issued for conversion of Series C Preferred Stock
  8,000 
  10,000 
Issuance of vested stock
  - 
  167 

4

Table of Contents

SANARA MEDTECH INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY (UNAUDITED)

 

 

Preferred Stock Series F

 

 

Common Stock

 

 

Additional

 

 

 

 

 

 

Total

 

 

 

$10 par value

 

 

$0.001 par value 

 

 

Paid-In

 

 

Accumulated

 

 

Noncontrolling

 

 

Shareholders'

 

 

 

 Shares

 

 

Amount

 

 

 Shares

 

 

Amount

 

 

Capital

 

 

Income/(Deficit)

 

 

Interest

 

 

Equity

 

Balance at December 31, 2019

 

 

1,136,815

 

 

$11,368,150

 

 

 

3,571,001

 

 

$3,571

 

 

$(2,081,829)

 

$(2,675,802)

 

$(221,690)

 

$6,392,400

 

Conversion of Preferred Shares to Common Stock

 

 

(1,136,815)

 

 

(11,368,150)

 

 

2,273,630

 

 

 

2,274

 

 

 

11,365,876

 

 

 

0

 

 

 

0

 

 

 

0

 

Conversion of Promissory Note to Common Stock

 

 

-

 

 

 

0

 

 

 

179,101

 

 

 

179

 

 

 

1,611,732

 

 

 

0

 

 

 

0

 

 

 

1,611,911

 

Share-based compensation

 

 

-

 

 

 

0

 

 

 

180,100

 

 

 

180

 

 

 

393,560

 

 

 

0

 

 

 

0

 

 

 

393,740

 

Net loss

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

 

 

 

 

(1,836,957)

 

 

(4,055)

 

 

(1,841,012)

Balance at March 31, 2020

 

 

-

 

 

$0

 

 

 

6,203,832

 

 

$6,204

 

 

$11,289,339

 

 

$(4,512,759)

 

$(225,745)

 

$6,557,039

 

Share-based compensation

 

 

-

 

 

 

0

 

 

 

(430)

 

 

(1)

 

 

186,172

 

 

 

0

 

 

 

0

 

 

 

186,171

 

Net loss

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

 

 

 

 

(1,125,764)

 

 

(3,793)

 

 

(1,129,557)

Balance at June 30, 2020

 

 

-

 

 

$0

 

 

 

6,203,402

 

 

$6,203

 

 

$11,475,511

 

 

$(5,638,523)

 

$(229,538)

 

$5,613,653

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Preferred Stock Series F

 

 

Common Stock

 

 

Additional

 

 

 

 

 

 

 

Total

 

 

 

$10 par value

 

 

$0.001 par value 

 

 

Paid-In

 

 

Accumulated

 

 

Noncontrolling

 

Shareholders' 

 

 

 

 Shares

 

 

Amount

 

 

 Shares

 

 

Amount

 

 

Capital

 

 

Income/(Deficit)

 

 

Interest

 

 

Equity

 

Balance at December 31, 2020

 

 

-

 

 

$-

 

 

 

6,297,008

 

 

$6,297

 

 

$13,176,576

 

 

$(7,032,242)

 

$(310,395)

 

$5,840,236

 

Issuance of common stock for asset acquisitions

 

 

-

 

 

 

0

 

 

 

50,370

 

 

 

50

 

 

 

1,749,950

 

 

 

0

 

 

 

0

 

 

 

1,750,000

 

Issuance of common stock in equity offering

 

 

-

 

 

 

0

 

 

 

1,265,000

 

 

 

1,265

 

 

 

28,937,992

 

 

 

0

 

 

 

0

 

 

 

28,939,257

 

Share-based compensation

 

 

-

 

 

 

0

 

 

 

4,744

 

 

 

5

 

 

 

325,513

 

 

 

0

 

 

 

0

 

 

 

325,518

 

Distribution to noncontrolling interest member

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

0

 

 

 

0

 

 

 

(200,000)

 

 

(200,000)

Net loss

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

0

 

 

 

(1,181,744)

 

 

(1,632)

 

 

(1,183,376)

Balance at March 31, 2021

 

 

-

 

 

$0

 

 

 

7,617,122

 

 

$7,617

 

 

$44,190,031

 

 

$(8,213,986)

 

$(512,027)

 

$35,471,635

 

Share-based compensation

 

 

-

 

 

 

0

 

 

 

(4,786)

 

 

(5)

 

 

297,927

 

 

 

0

 

 

 

0

 

 

 

297,922

 

Capital contribution of noncontrolling interest member

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

0

 

 

 

0

 

 

 

93,879

 

 

 

93,879

 

Net loss

 

 

-

 

 

 

0

 

 

 

-

 

 

 

0

 

 

 

 

 

 

 

1,171,492)

 

 

(34,481)

 

 

(1,205,973)

Balance at June 30, 2021

 

 

-

 

 

$-

 

 

 

7,612,336

 

 

$7,612

 

 

$44,487,958

 

 

$(9,385,478)

 

$(452,629)

 

$34,657,463

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.


Wound Management Technologies,

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SANARA MEDTECH INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS (UNAUDITED)

 

 

Six Months Ended

 

 

 

June 30,

 

 

 

2021

 

 

2020

 

 

 

 

 

 

 

 

Cash flows from operating activities:

 

 

 

 

 

 

Net loss

 

$(2,389,349)

 

$(2,970,569)

Adjustments to reconcile net loss to net cash used in operating activities

 

 

 

 

 

 

 

 

Depreciation and amortization

 

 

191,398

 

 

 

127,726

 

Interest expense on convertible debt

 

 

0

 

 

 

8,354

 

Interest expense on PPP loan

 

 

0

 

 

 

1,101

 

Loss on disposal of asset

 

 

0

 

 

 

2,180

 

Bad debt expense

 

 

51,536

 

 

 

30,000

 

Inventory obsolescence

 

 

29,834

 

 

 

75,422

 

Share-based compensation

 

 

623,440

 

 

 

491,069

 

Noncash lease expense

 

 

61,629

 

 

 

57,880

 

Loss on equity method investment

 

 

278,904

 

 

 

0

 

 

 

 

 

 

 

 

 

 

Changes in operating assets and liabilities:

 

 

 

 

 

 

 

 

Accounts receivable

 

 

(279,229)

 

 

(112,301)

Inventory

 

 

(419,979)

 

 

(191,595)

Prepaid - related parties

 

 

0

 

 

 

(50,970)

Prepaid and other assets

 

 

114,707

 

 

 

(310,666)

Accounts payable

 

 

42,318

 

 

 

(197,709)

Accounts payable - related parties

 

 

(166,081)

 

 

(66,346)

Accrued royalties and expenses

 

 

25,327

 

 

 

333,731

 

Accrued liabilities

 

 

239,650

 

 

 

40,502

 

Net cash used in operating activities

 

 

(1,595,895)

 

 

(2,732,191)

 

 

 

 

 

 

 

 

 

Cash flows from investing activities:

 

 

 

 

 

 

 

 

Purchase of property and equipment

 

 

(25,446)

 

 

(57,456)

Purchase of intangible assets

 

 

0

 

 

 

(1,100,000)

Investment in equity securities

 

 

(3,184,278)

 

 

0

 

Net cash used in investing activities

 

 

(3,209,724)

 

 

(1,157,456)

 

 

 

 

 

 

 

 

 

Cash flows from financing activities:

 

 

 

 

 

 

 

 

Draw on line of credit

 

 

800,000

 

 

 

0

 

Pay off line of credit

 

 

(800,000)

 

 

0

 

Proceeds from PPP Loan

 

 

0

 

 

 

583,000

 

Public offering net proceeds

 

 

28,939,257

 

 

 

0

 

Distribution to noncontrolling interest shareholders

 

 

(200,000)

 

 

0

 

Net cash provided by financing activities

 

 

28,739,257

 

 

 

583,000

 

 

 

 

 

 

 

 

 

 

Net increase (decrease) in cash

 

 

23,933,638

 

 

 

(3,306,647)

Cash, beginning of period

 

 

455,366

 

 

 

6,611,928

 

Cash, end of period

 

$24,389,004

 

 

$3,305,281

 

 

 

 

 

 

 

 

 

 

Cash paid during the period for:

 

 

 

 

 

 

 

 

Interest

 

$711

 

 

$0

 

Income taxes

 

 

0

 

 

 

0

 

 

 

 

 

 

 

 

 

 

Supplemental noncash investing and financing activities:

 

 

 

 

 

 

 

 

Common stock issued for conversion of Series F Preferred Stock

 

 

0

 

 

 

11,368,150

 

Common stock issued for conversion of related party debt and interest

 

 

0

 

 

 

1,611,911

 

Common stock issued for asset acquisitions

 

 

1,750,000

 

 

 

750,000

 

License agreement as capital contribution from noncontrolling interest member

 

 

93,879

 

 

 

0

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.

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SANARA MEDTECH INC. AND SUBSIDIARIES

NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS

NOTE 1 – NATURE OF BUSINESS AND BACKGROUND

Sanara MedTech Inc. (“we”, “our”, the “Company”) is a medical technology company focused on developing and Subsidiaries

Notescommercializing transformative technologies to Unaudited Consolidated Financial Statements
Note 1 - Summaryimprove clinical outcomes and reduce healthcare expenditures in the surgical and chronic wound and skin care markets. The Company’s portfolio of Significant Accounting Policies
products and services is designed to allow us to deliver comprehensive wound and skin care solutions for patients in all care settings, including acute (hospitals and long-term acute care hospitals) and post-acute (wound care clinics, physician offices, skilled nursing facilities (“SNFs”), home health, hospice, and retail). 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 wound and skin care products and technologies.

Impact of the COVID-19 Pandemic

Beginning in March 2020, many states issued orders suspending elective surgeries in order to free-up hospital resources to treat COVID-19 patients. This resulted in a reduction in demand for the Company’s surgical products beginning in the second half of March 2020. Additionally, most states limited access to SNFs to only resident caregivers, which impeded the Company’s ability to provide education and product training to the clinicians who use the Company’s products in these facilities. These restrictions resulted in an overall decline in sales for the second quarter of 2020. During the second half of 2020 and the first half of 2021, the Company saw a strong rebound in product sales as restrictions on elective surgeries eased in its primary markets in Texas, Florida, and the southeastern United States.

Due to recent COVID-19 resurgences and variants, the duration and effects of the pandemic remain uncertain; however, management believes that elective surgical procedures will continue to be performed with the exception of certain geographic hotspots. The Company continues to closely monitor the pandemic in order to ensure the safety of the Company’s people and its ability to serve its customers and patients.

NOTE 2 -- SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of Presentation

The terms “WMT,” “we,” “the Company,” and “us” as used in this report refer to Wound Management Technologies, Inc.

The accompanying unaudited consolidated balance sheet as of September 30, 2017, and unaudited consolidatedfinancial statements of operations for the nine months ended September 30, 2017 and 2016, 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 of the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. Certain prior period amounts in the consolidated financial statements and accompanying notes have been reclassified to conform to the current period’s presentation. In the opinion of management of WMT,the Company, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included. Operating results for the three and nine-month periodssix-month period ended SeptemberJune 30, 2017,2021, are not necessarily indicative of the results that may be expected for the year ending December 31, 2017,2021, or any other period. These financial statements and notes should be read in conjunction with the financial statements for each of the two years ended December 31, 2016,2020, and December 31, 2015,2019, included in the Company’s most recent Annual Report on Form 10-K. The accompanying consolidated balance sheet as of December 31, 2016, has been derived from the audited financial statements filed in our Form 10-K and is included for comparison purposes in the accompanying balance sheet. Certain prior year amounts have been reclassified to conform to current year presentation.

Principles of Consolidation

The accompanying unaudited consolidated financial statements include the accounts of WMT andSanara MedTech Inc., its wholly-owned subsidiaries:  Wound Care Innovations, LLCand majority-owned subsidiaries, as well as other entities in which the Company has a Nevada limited liability company (“WCI”); Resorbable Orthopedic Products, LLC, a Texas limited liability company (“Resorbable);controlling financial interest.  All significant intercompany profits, losses, transactions and Innovate OR, Inc. “InnovateOR” formerly referred to as BioPharma Management Technologies, Inc., a Texas corporation (“BioPharma”). All intercompany accounts and transactionsbalances have been eliminated.

eliminated in consolidation.

Use of Estimates

The preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect amounts reported in the financial statements and accompanying notes. The extent to which the COVID-19 pandemic may directly or indirectly impact our business, financial condition, and results of operations is highly uncertain and subject to change. The Company considered the potential impact of the COVID-19 pandemic on its estimates and assumptions and determined there was not a material impact on the Company’s estimates and assumptions used in preparing the unaudited consolidated financial statements as of and for the six months ended June 30, 2021. However, actual results could differ from those estimates and there may be changes to the Company’s estimates in future periods.

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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 per share in accordance with Accounting Standards Codification (“ASC”) Topic 260, Earnings per Share, which requires the Company to present basic and dilutive 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 similar 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 current and prior period calculations, as their inclusion would have been anti-dilutive during the three and six months ended June 30, 2021 and 2020 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 three and six months ended June 30, 2021 and 2020 as such shares would have had an anti-dilutive effect:

 

 

As of June 30,

 

 

 

2021

 

 

2020

 

 

 

 

 

 

 

 

Stock options

 

 

11,500

 

 

 

11,500

 

Unvested restricted stock

 

 

115,719

 

 

 

154,090

 

Revenue Recognition

The Company recognizes revenue in accordance with ASC Topic 606, Revenue from Contracts with Customers (“ASC 606”), which the Company adopted on January 1, 2018 using the modified retrospective method. Revenues are recognized when 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 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 2020 or 2021.

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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 one performance obligation exists.

Recognition of revenue as performance obligations are satisfied

Product revenues are recognized when 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 six months ended June 30, 2021 and 2020. All revenue was generated in the United States; therefore, no geographical disaggregation was necessary.

 

 

Six Months Ended

 

 

 

June 30,

 

 

 

2021

 

 

2020

 

Product sales revenue

 

$11,186,069

 

 

$6,391,014

 

Royalty revenue

 

 

100,500

 

 

 

100,500

 

Total Revenue

 

$11,286,569

 

 

$6,491,514

 

The Company recognizes royalty revenue from a development and licensing agreement between BioStructures, LLC and the Company. The Company records revenue each calendar quarter as earned per the terms of the agreement which stipulates that 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 throughout the life of the patent which expires in 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).

Contract Assets and Liabilities

The Company does not have any contract assets or contract liabilities.

Allowance for Doubtful Accounts

The Company establishes an allowance for doubtful accounts to ensure accounts receivable are not overstated due to uncollectible accounts. The Company recorded bad debt expense of $51,536 and $30,000during the six months ended June 30, 2021 and 2020, respectively. The allowance for doubtful accounts was $120,273 at June 30, 2021 and $64,989 at December 31, 2020. Bad debt reserves are maintained based on a variety of factors, including the length of time receivables are past due and a detailed review of certain individual customer accounts. The Company also establishes other allowances to ensure accounts receivable are not overstated due to customer rebates and product returns. These allowances totaled $18,144 at June 30, 2021 and $35,200 at December 31, 2020. If circumstances related to customers change, estimates of the recoverability of receivables would be further adjusted. The Company considered the impact of COVID-19 in its analysis of receivables and determined its accounts receivable allowances were appropriate at June 30, 2021.

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 of finished goods and related packaging supplies.components. The Company recorded inventory obsolescence expense of $0 for$29,834 the three months and $8,347 for the ninesix months ended SeptemberJune 30, 2017, compared to $15,631 for2021 and $75,422 the ninesix months ended SeptemberJune 30, 2016.2020. The allowance for obsolete and slow-moving inventory had a balance of $116,772$295,841 at SeptemberJune 30, 2017,2021, and $153,023$276,603 at December 31, 2016.

2020. The Company considered the impact of COVID-19 on its recorded value of inventory and determined no adjustment was necessary as of June 30, 2021.

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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 three to ten years. Below is a summary of property and equipment for the periods presented:

 

 

June 30,

 

 

December 31,

 

 

 

2021

 

 

2020

 

Computers

 

$98,140

 

 

$87,252

 

Office equipment

 

 

22,598

 

 

 

22,597

 

Furniture and fixtures

 

 

209,746

 

 

 

205,871

 

Leasehold improvements

 

 

2,030

 

 

 

2,030

 

Internal use software

 

 

1,485,530

 

 

 

485,530

 

Capital in progress

 

 

10,682

 

 

 

0

 

 

 

 

1,828,726

 

 

 

803,280

 

Less accumulated depreciation

 

 

(159,732)

 

 

(124,691)

 

 

 

 

 

 

 

 

 

Property and equipment, net

 

$1,668,994

 

 

$678,589

 

Depreciation expense related to property and equipment was $35,040 for the six months ended June 30, 2021, and $33,227 for the six months ended June 30, 2020.

The Company considered the impact the COVID-19 pandemic may have had on the carrying value of its property and equipment and determined that no impairment loss had occurred as of June 30, 2021. The Company will continue to assess the COVID-19 pandemic’s impact on its business including any indicators of impairment of property and equipment.

Internal Use Software

The Company accounts for costs incurred to develop 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 amortized over the estimated useful life of the software, which is generally five to seven years.

Intangible Assets

Intangible assets are stated at cost of acquisition less accumulated amortization and impairment loss, if any. Cost of acquisition includes purchase price and any cost directly attributable to bringing the asset to its working condition for the intended use. The Company amortizes its intangible assets on a straight-line basis over the useful life of the respective assets which is generally the life of the related patents (if applicable).

See Note 3 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, including the COVID-19 pandemic, 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 net realizable value. No impairment was recorded during the six months ended June 30, 2021 and 2020.

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Table of Contents

Investments in Equity Securities

The Company’s equity investments consist of non-marketable equity securities in privately held companies without readily determinable fair values, and 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 our consolidated statements of operations. The Company’s equity method investments are 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 equity method investments using the cumulative earnings approach on the consolidated statements of cash flows.

The Company has reviewed the carrying value of its investments and has determined there was no impairment or observable price changes as of June 30, 2021.

Fair Value Measurements

Measurement

As defined in Accounting Standards CodificationASC Topic 820, Fair Value Measurement (“ASC”ASC 820”) Topic No. 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 Topic No. 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 of 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 non-exchange-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.

On July 25, 2017,

The carrying amounts of cash, accounts receivable, accounts payable and accrued expenses approximate fair value because of the stock purchase warrants relatedshort-term nature of these instruments. The Company does not have any assets or liabilities that are required to be measured and recorded at fair value on a recurring basis.

Income Taxes

Income taxes are accounted for under the remaining derivativeasset 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 expired and on September 30, 2017,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 of the deferred tax asset will not be realized.

Advertising Expense

In accordance with ASC Topic No. 720-35-25-1, the Company had no derivative liabilities related to stock purchase warrants.

Our intangible assets have also been valued usingrecognizes advertising expenses the fair value accounting treatment and a description offirst time the methodology used, including the valuation category, is described in the Company’s Annual Report on Form 10-K.
Income (Loss) Per Share
advertising takes place. Advertising expenses are expensed as incurred.

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Share-based Compensation

The Company computes income (loss) per shareaccounts for stock-based compensation to employees and nonemployees in accordance with Accounting Standards Codification “ASC”Update (“ASU”) 2018-07 Topic No. 260, “Earnings per Share,” which requires718. 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 to present basicestimates the fair value of stock-based payments using the Black-Scholes option-pricing model for common stock options and dilutive income (loss) per share when the effect is dilutive. Basic income (loss) per share is computed by dividing income (loss) available to common stockholders by the weighted average number of common shares available. Diluted income (loss) per share is computed similar to basic income (loss) per share except that the denominator is increased to include the number of additional common shares that would have been outstanding if the potential common shares had been issued and if the additional common shares were dilutive. All convertible instruments were excluded as their inclusion would have been anti-dilutive during both the three months and nine months ended September 30, 2017warrants, and the nine months ended September 30, 2016. The dilutive effectclosing price of the outstanding convertible preferredCompany’s common stock for common stock issuances.

Research and Development Costs

Research and development expenses include costs for contracted services related to improvements to manufacturing processes, enhancements to the three months ended September 30, 2016 was 85,689,772 sharesCompany’s currently available products, and an adjustment to net income of $75,032.

additional investments in the product and platform development pipeline. The Company expenses research and development costs as incurred.

Recently IssuedAdopted Accounting Pronouncements

In May 2014,December 2019, the Financial Accounting Standards Board (FASB) issued ASU 2019-12, Simplifications to Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customersfor Income Taxes, which isremoves certain exceptions to bethe general principles of Topic 740 and adds guidance to reduce complexity in accounting for income taxes. The ASU is effective for reportingannual and interim periods in fiscal years beginning after December 15, 2017. 2020. The adoption of this standard did not have a material effect on the Company’s consolidated financial statements.

NOTE 3 – INTANGIBLE ASSETS

The carrying values of the Company’s finite-lived intangible assets were as follows:

 

 

June 30, 2021

 

 

December 31, 2020

 

 

 

 

 

 

Accumulated

 

 

 

 

 

 

 

 

Accumulated

 

 

 

 

 

 

Cost

 

 

Amortization

 

 

Net

 

 

Cost

 

 

Amortization

 

 

Net

 

Product Licenses

 

$4,193,879

 

 

$(417,519)

 

$3,776,360

 

 

$3,350,000

 

 

$(264,909)

 

$3,085,091

 

Patent

 

 

510,310

 

 

 

(510,310)

 

 

0

 

 

 

510,310

 

 

 

(510,310)

 

 

0

 

Software and Other

 

 

64,464

 

 

 

(55,637)

 

 

8,827

 

 

 

64,464

 

 

 

(51,889)

 

 

12,575

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total

 

$4,768,653

 

 

$(983,466)

 

$3,785,187

 

 

$3,924,774

 

 

$(827,108)

 

$3,097,666

 

In March 2021, the Company issued 20,834 shares of its common stock to Rochal Industries, LLC (“Rochal”) for a $750,000 milestone payment required per the terms of a licensing agreement with Rochal. The payment became due upon the Company’s public offering of common stock in February 2021. The milestone payment was recorded as an addition to intangible assets.

As of June 30, 2021, the weighted-average amortization period for all intangible assets was 12.4 years. Amortization expense related to intangible assets was $156,358 for the six months ended June 30, 2021 and $94,499 for the six months ended June 30, 2020. The estimated remaining amortization expense as of June 30, 2021 is as follows:

Remainder of 2021

 

$172,769

 

2022

 

 

343,123

 

2023

 

 

338,043

 

2024

 

 

338,043

 

2025

 

 

338,043

 

Thereafter

 

 

2,255,166

 

Total

 

$3,785,187

 

The Company has reviewed the pronouncementcarrying value of intangible assets due to the events and believes it willcircumstances surrounding the COVID-19 pandemic. The Company does not have a materialbelieve the impact of COVID-19 has created an impairment loss on the Company’s financial position, operations or cash flows.

In February 2016, the FASB issued ASC 842 Leases which is to be effective for reporting periods beginning after December 15, 2018. The Company is currently reviewing any impact that it will haveintangible assets as of June 30, 2021. Accordingly, there was no impairment loss recognized on the Company’s financial position, operations or cash flows.
Note 2 - Going Concern
The Company has continuously incurred losses from operations, however, the operating loss in 2016 included a significant nonrecurring expense in the amount of $818,665, primarily a non-cash loss on the issuance of warrants for services valued at $758,665. Without this non-cash expense, operating income was $342,918 for 2016. The Company has a working capital deficit of $448,630 on September 30, 2017, and surplus of $601,654 on December 31, 2016. The Company has adopted a robust operating plan for 2017 that projects existing cash and future cash to be generated from operations will satisfy our foreseeable working capital, debt repayment and capital expenditure requirements for at least the next twelve months. However, minimal funding may be required at certain timesintangible assets during the year due to the timing of significant expenditures such as inventory purchases. The Company obtained $50,050 cash proceeds from the issuance of series C preferred stock during the ninesix months ended SeptemberJune 30, 2017,2021.

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NOTE 4 - COMMITMENTS AND CONTINGENCIES

License Agreements and believes it will be able to obtain any such additional funding, if required during the remainder of 2017. We will also monitor our cash flow; assess our business plan; and make expenditure adjustments accordingly. Based upon the Company's current ability to obtain additional financing or equity capital and to achieve profitable operations, it is not appropriate at this time to continue using the going concern basis.

Note 3 – Accounts Payable and Notes Payable
Accounts Payable
During the nine months ended September 30, 2017, the WMTI reached an agreement to settle an outstanding payable with WellDyne Health, LLC, (“WellDyne”), a third party that had provided shipping and consulting services on behalf of the Company effective through September 19, 2015. As part of that settlement, WellDyne forgave $39,709 of the outstanding payable.

Notes Payable
During the nine months ended September 30, 2017, the Company paid a total of $190,838 principal and $10,937 in accrued interest to three non-related party note holders and reached an agreement with them to forgive $10,937 in accrued interest. As a result, all three of these notes were retired. As of September 30, 2017, the balance consists of one note in the amount of $223,500. See Note 9 Subsequent Events for a discussion of the disposition of this note payable.
Convertible Notes Payable - Related Parties
Royalties

CellerateRX® Activated Collagen®

On June 15, 2015,August 27, 2018, the Company entered into an exclusive, world-wide sublicense agreement with CGI Cellerate RX, LLC (“CGI Cellerate RX”) to distribute CellerateRX Surgical and HYCOL products into the wound care and surgical 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 on January 26, 2021, the term loan agreementsof 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. Minimum royalties of $400,000 per year are payable for the first five years of the sublicense agreement.

For the six months ended June 30, 2021 and 2020, royalty expense accrued under the terms of this agreement totaled $404,220 and $210,220, respectively.

BIAKŌS Antimicrobial Wound Gel and BIAKŌS Antimicrobial Skin and Wound Cleanser

On July 7, 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 (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) approved. The James W. Stuckert Revocable Trust (“SRT)Company’s Executive Chairman is a director of Rochal, and The S. Oden Howell Revocable Trust (“HRT”),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.

Recent and future commitments under the terms of the BIAKŌS License Agreement include:

In March 2021, the Company issued 20,834 shares of its common stock to Rochal as full payment of a $750,000 milestone which became due upon the Company’s public offering of common stock in February 2021.

The Company pays Rochal a royalty of 2-4% of net sales. The minimum annual royalty due to Rochal was $100,000 in 2020 and will increase by 10% 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.

For the six months ended June 30, 2021 and 2020, royalty expense recognized under this agreement was $55,000 and $50,000, respectively.

CuraShield Antimicrobial Barrier Film and No Sting Skin Protectant

On October 1, 2019, the Company executed a license agreement with Rochal pursuant to which SRT made a loan to 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.

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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 have been recognized under this agreement as of June 30, 2021.

Debrider License Agreement

On May 4, 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:

At the time Rochal issues a purchase order to its contract manufacturer for the first good manufacturing practice run of the licensed products, the Company will pay Rochal $600,000 in cash.

Upon FDA clearance of the licensed products, the Company will pay Rochal $500,000 in cash and $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 June 30, 2021.

Resorbable Bone Hemostat

The Company acquired a patent in 2009 for a resorbable bone hemostat and delivery system for orthopedic bone void fillers. 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 3% royalty on product sales over the life of the patent, which expires in 2023, with annual minimum royalties of $201,000. The Company pays two unrelated third parties a combined royalty equal to 8% of the Company’s net revenues or minimum royalties generated from products that utilize the Company’s acquired patented bone hemostat and delivery system. To date, royalties 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 under the terms of the license agreement has been $16,080 ($4,020 per quarter).

Other Commitments

At the time of the formation of Sanara Pulsar, it and Wound Care Solutions, Limited (“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. In 2019, the Company advanced to WCS $200,000 and recorded the payment as a reduction of non-controlling interests. In the event WCS’s Form K-l from Sanara Pulsar for the year 2020 does not allocate to WCS net income of at least $200,000 (the “Target Net Income”), then Cellerate, LLC will, within 30 days after such determination, pay WCS the amount of $600,000funds representing the difference between the Target Net Income and HRT made a loanthe actual amount of net income shown on WCS’s Form K-1 for the year 2020. In March 2021, the Company paid WCS $200,000 for the year 2020. For each of the years 2021 through 2024 the Target Net Income will increase by 10%, and in the event WCS’s Form K-1 for any of those years does not allocate to WCS net income in an amount at least equal to the Company inTarget Net Income for such year, then Cellerate, LLC will, within 30 days after such determination, pay WCS the amount of $600,000 under Senior Secured Convertible Promissory Notes (the “Notes”). Both SRTfunds representing the difference between the Target Net Income and HRTthe actual amount of net income shown on WCS’s Form K-1 for the applicable year. All other distributions made by Sanara Pulsar to its members, not including tax distributions, will be made exclusively to Cellerate, LLC until such time as Cellerate, LLC has received an amount of distributions equal to all such advances to WCS.

NOTE 5 - OPERATING LEASES

The Company periodically enters into operating lease contracts for office space and equipment. Arrangements are controlled by affiliatesevaluated at inception to determine whether such arrangements constitute a lease.

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Right of use assets, which we refer to as “ROU assets,” represent the Company. 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 Notes each carryCompany has two operating leases: an interestoffice space lease with a remaining lease term of 36 months and a copier lease with a remaining lease term of one month as of June 30, 2021. All other leases are short-term leases, which for practical expediency, the Company has elected to not recognize as lease assets and lease liabilities.

In accordance with ASC Topic 842, the Company has recorded lease assets of $406,024 and a related lease liability of $419,052 as of June 30, 2021. The Company recorded amortization expense of $ 61,629 for the six months ended June 30, 2021 for its leased assets. Cash paid for amounts included in the measurement of operating lease liabilities as of June 30, 2021 was $76,178. The present value of our operating lease liabilities is shown below.

Maturity of Operating Lease Liabilities

 

 

June 30, 2021

 

Remainder of 2021

 

$75,139

 

2022

 

 

151,333

 

2023

 

 

154,271

 

2024

 

 

77,870

 

2025

 

 

0

 

Thereafter

 

 

0

 

 

 

 

 

 

Total lease payments

 

 

458,613

 

Less imputed interest

 

 

(39,561)

Present Value of Lease Liabilities

 

$419,052

 

 

 

 

 

 

Operating lease liability - current

 

 

128,301

 

Operating lease liability – long term

 

 

290,751

 

As of June 30, 2021, our operating leases have a weighted average remaining lease term of 3.0 years and a weighted average discount rate of 10% per annum,6.25%.

NOTE 6 – SHAREHOLDERS’ EQUITY

Preferred Stock

On February 7, 2020, CGI Cellerate RX, an affiliate of The Catalyst Group, Inc. (“Catalyst”), converted its entire holdings of its 30-month $1,500,000 convertible promissory note and (subject to various default provisions) all unpaid principal and accrued but unpaid interest under the Notes is due and payable on June 15, 2018. The Notes may be prepaid in whole or in part upon ten days’ written notice, and all unpaid principal and accrued interest under the Notes may be converted, at the option1,136,815 shares of SRT and HRT,Series F Convertible Preferred Stock into shares of the Company’s Series C Convertible Preferred Stock at a conversion pricecommon stock. The Company issued an aggregate of $70.00 per share at any time prior to maturity.”). The Company’s obligations under2,452,731 shares of common stock in the two notes are secured by all the assetsconversions. As of the CompanyJune 30, 2021, Catalyst and its subsidiaries.

Note 4 – Commitments and Contingencies
Royalty agreements.
Effective November 28, 2007, WCI entered into separate exclusive license agreements with Applied Nutritionals, LLC (“Applied”) and its founder George Petito, pursuant to which WCI obtainedaffiliates controlled the exclusive world-wide license to make products incorporating intellectual property covered byvoting of a patent related to CellerateRX products. In consideration for the licenses, WCI agreed to pay to Applied the following royalties, beginning January 3, 2008: (a) an upfront royalty of $100,000 in the aggregate, (b) an aggregate royalty of fifteen percent (15%) of gross sales occurring during the first year of the license; (c) an additional upfront royalty of $400,000, in the aggregate, which was paid October, 2009; plus (d) an aggregate royalty of three percent (3%) of gross sales for all sales occurring after the payment of the $400,000 upfront royalty. In addition, WCI must maintain a minimum aggregate annual royalty payment of $375,000 for 2009 and thereafter, if the royalty payments made do not meet or exceed that amount. The total of unpaid royalties as of December 31, 2016, was $276,916, and it was paid in full in January of 2017. As of September 30, 2017, the balance of accrued royalties for the current year is $232,511.
On September 29, 2009, the Company entered into an Asset Purchase Agreement (the “Asset Purchase Agreement”), by and among the Company, RSIACQ, LLC, a wholly-owned subsidiary of the Company (RSI), Resorbable Orthopedic Products, LLC (“Resorbable”) and Resorbable’s members, pursuant to which, RSI acquired substantially all of Resorbable’s assets, in exchange for (i) 500,0003,497,421 shares of the Company’s common stock, and (ii) a royalty equal to eight percent (8%)which represented 46% of the net revenues generated from products sold by7,612,336 shares of common stock outstanding.

Common Stock

At the Company’s Annual Meeting of Shareholders held on July 9, 2020, the Company or anyapproved 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 its affiliates, which products are developed from or otherwise utilize any248,234 shares had been issued under the LTIP Plan and 1,751,766 were available for issuance as of the patented technology acquired from Resorbable. The royalty is paid to Barry Constantine Consultants, LLC for distribution to the original patent holders, (including Mr. Barry Constantine) and/or their heirs. The royalty expense was $12,060 for each of the nine-months ended SeptemberJune 30, 2017, and September 30, 2016, and $4,020 for each of the three-months ended September 30, 2017 and September 30, 2016. Mr. Constantine resigned effective October 1, 2017, as a contract employee of2021.

On January 18, 2021, the Company in which he held the position of Director of R&D.

Evolution Partners LLC Letter Agreement and Termination Agreement
On October 10, 2017, Wound Management Technologies, Inc. (the “Company”) and Evolution Venture Partners LLC (“EVP”) entered into a termination agreementan Equity Exchange Agreement (the “Termination“Exchange Agreement”) terminating,, effective as of September 29, 2017, that certain letter agreement dated April 26, 2016, (the “Agreement”January 14, 2021, with two individuals who each owned 50% of the outstanding equity interests in Woundyne Medical, LLC (“Woundyne”), by and between. Pursuant to the Exchange Agreement, the Company EVP, and Middlebury Securities, LLC (“Middlebury”). Middlebury terminated its charter on or about July 27, 2016, and therefore is not a party to the Termination Agreement. The Agreement had an initial term of one year (with an automatic six-month renewal term) and provided for:
· A $60,000 consulting fee payable upon executionacquired 100% of the Agreement, refundable only upon cancellationissued and outstanding equity interests of the Agreement by EVP during the initial one-year term.
· A success feeWoundyne in an amount equal to 5% of the transaction value of any strategic transaction.
· A selling fee equal to 3% of the gross proceeds of any debt financing transaction or 5% of the gross proceeds of any equity financing transaction.
· The issuance to EVP of a warrant (the “Warrant”)exchange for the purchaseissuance of 60,000,000an aggregate of 29,536 shares of the Company’s common stock parwith a fair value $0.001of $1,000,000. The acquisition of the outstanding equity interests of Woundyne was accounted for as an asset acquisition. The primary asset acquired by the Company is the Woundyne software platform which allows data related to chronic and surgical wounds to be tracked, monitored, and interfaced with the software user’s electronic medical records. Woundyne has no other material assets, liabilities, or revenues. The issuance of these shares was capitalized as internal use software. The Company subsequently changed the name of Woundyne Medical, LLC to WounDerm, LLC.

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On February 12, 2021, the Company entered into an underwriting agreement (the “Underwriting Agreement”) with Cantor Fitzgerald & Co. as representative of several underwriters named therein (collectively, the “Underwriters”), pursuant to which the Company agreed to issue and sell an aggregate of 1,100,000 shares of the Company’s common stock to the Underwriters at a price to the public of $25.00 per share, (“Common Stock”less underwriting discounts and commissions (the “Offering”),. Pursuant to the Underwriting Agreement, the Company granted the Underwriters a 30-day option to purchase up to an additional 165,000 shares of common stock at an exercisethe public offering price, of $0.12 per share.


less underwriting discounts and commissions, which the Underwriters exercised in full. The total amountOffering, including the purchase of the consulting fee165,000 additional shares of common stock, closed on February 17, 2021.

The net proceeds to the Company from the Offering were $28.9 million, after (i) giving effect to the Underwriter’s full exercise of its option to purchase additional shares of common stock, and warrant expense was $818,665(ii) deducting the underwriting discounts and is recognizedcommissions and offering expenses payable by the Company. Through an insured cash sweep service, the net proceeds have been deposited in 2016 as “Other administrative expenses” inaccounts insured by the Consolidated Statement of Operations.

AsFederal Deposit Insurance Corporation. 

Following the closing of the termination date, there were no Financing Transactions or Strategic TransactionsOffering in February of 2021, the Company made the $750,000 Post Capital Raise Payment (as defined in the BIAKŌS License Agreement) being considered byto Rochal in the form of 20,834 shares of the Company’s common stock (see Notes 3 and 4).

On July 14, 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. The acquired assets were purchased for an aggregate purchase price of approximately $1,000,000 consisting of (i) approximately $500,000 in cash and no such transactions occurred.

Pursuant(ii) 14,369 shares of the Company’s common stock, representing an amount equal to $500,000 based on the Termination Agreement, EVP has agreed to cancelaverage closing sale price of the Warrant in exchangeCompany’s common stock for the Company’s issuancetwenty trading days immediately preceding July 14, 2021. See Note 10 for more information regarding this transaction.

Restricted Stock Awards

During the six months ended June 30, 2021, the Company granted and issued 4,744shares of restricted common stock to EVP of 750,000one employee under the LTIP Plan. The shares of Common Stock. There was no incremental increaseare subject to certain vesting provisions and other terms and conditions set forth in the employee’s restricted stock agreement. The fair value of this award was $216,658 based on the modified stock-based compensation award asclosing price of the modificationCompany’s common stock on the grant date and accordingly, no additionalis recognized as compensation cost was recognized.

Office leases
In March of 2017, the Company executed a new office lease for office space located at 1200 Summit Ave., Suite 414, Fort Worth, TX 76102 and relocated our corporate offices there on April 22, 2017. The lease is effective May 1, 2017, and ends on the last day of the fiftieth (50th) full calendar month following the effective date, (June 30, 2021). Monthly base rental payments are as follows: months 1-2, $0; months 3-14, $7,250; months 15-26, $7,401; months 27-38, $7,552; and months 39-50, $7,703. Rent expense is recognized on a straight-line basis over the termvesting period of the Leaseaward.

Share-based compensation expense of $623,440 was recognized in selling, general and administrative expenses during the six months ended June 30, 2021, compared to $491,069 recognized during the six months ended June 30, 2020.

At June 30, 2021, there was $1,001,684 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 0.8 years.

Below is a summary of restricted stock activity for the six months ended June 30, 2021:

 

 

For the Six Months Ended

 

June 30, 2021

 

 

 

 

Weighted

Average

 

 

Shares 

 

Grant Date

Fair Value

Non-vested at beginning of period

 

 

170,178

 

 

$14.20

 

Granted

 

 

4,744

 

 

 

45.67

 

Vested

 

 

(54,417)

 

 

15.51

 

Forfeited

 

 

(4,786)

 

 

13.03

 

Non-vested at June 30, 2021

 

 

115,719

 

 

$14.92

 

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Stock Options

A summary of the status of outstanding stock options at June 30, 2021 and changes during the six-month period then ended is presented below:

 

 

For the Six Months Ended

 

June 30, 2021

 

 

 

 

 

Weighted Average

 

 

Weighted Average

 

 

Options

 

 

Exercise Price

Remaining Contract Life

 

Outstanding at beginning of period

 

 

11,500

 

 

$6.00

 

 

 

 

Granted

 

 

-

 

 

 

0

 

 

 

 

Exercised

 

 

-

 

 

 

0

 

 

 

 

Forfeited

 

 

-

 

 

$0

 

 

 

 

Expired

 

 

-

 

 

 

0

 

 

 

 

Outstanding at June 30, 2021

 

 

11,500

 

 

$6.00

 

 

 

1.5

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Exercisable at June 30, 2021

 

 

11,500

 

 

$6.00

 

 

 

1.5

 

NOTE 7 – DEBT AND CREDIT FACILITIES

Revolving Line of Credit

In December 2018, Cellerate, LLC executed agreements with Cadence Bank, N.A.(“Cadence”) which provided Cellerate, LLC access to a revolving line of credit up to a maximum principal amount of $1,000,000. The line of credit was used to support the short-term working capital requirements of Cellerate, LLC. On June 21, 2019, the Company modified the revolving line of credit with Cadence to increase the maximum principal amount from $1,000,000 to $2,500,000. On October 16, 2019, the Company paid down the entire $2,200,000 balance of the revolving line of credit with cash proceeds received from a private placement of the Company’s common stock. This revolving line of credit matured on June 19, 2020.

On January 15, 2021, the Company entered into a loan agreement (the “Loan Agreement”) with Cadence providing for a $2.5 million revolving line of credit. The revolving line of credit matures on January 13, 2023 and is secured by substantially all of the Company’s assets. Any amounts outstanding will bear interest of 0.75% plus the “Prime Rate” designated in the “Money Rates” section of the Wall Street Journal. Proceeds from the line of credit are to be used to provide the Company with additional working capital in support of current assets and for other general corporate purposes and may not be used for acquisitions.

The line of credit contains customary representations and warranties and requires the Company to maintain compliance with certain financial covenants, including, among others, a minimum liquidity of $1,000,000 as of December 31, 2020 and March 31, 2021, a minimum Tangible Net Worth (as defined in the Loan Agreement) of $1,000,000 and, beginning with the fiscal quarter ended June 30, 2021, a minimum Interest Coverage Ratio (as defined in the Loan Agreement) of 1.5 to 1.0. The Loan Agreement also contains customary events of default. If such an event of default occurs, Cadence would be entitled to take various actions, including the acceleration of amounts due under the Loan Agreement. The Company generally may (and must, under certain circumstances) prepay all or a portion of the principal outstanding on the revolving line of credit prior to its contractual maturity.

On February 11, 2021, the Company made an $800,000 draw on the revolving line of credit. On February 19, 2021, the Company paid down the entire balance of the revolving line of credit. As of June 30, 2021, there were no outstanding amounts owed by the Company under the Loan Agreement.

On June 29, 2021, the Company amended the revolving line of credit with Cadence to modify certain financial covenants which included changing the initial measurement period of the minimum Interest Coverage Ratio (as defined in the Loan Agreement) from June 2021 to March 2022 (the “Modification Agreement”). In connection with this change, beginning with the fiscal quarter ended June 30, 2021 through the fiscal quarter ending December 31, 2021, the required minimum Tangible Net Worth (as defined in the Loan Agreement) was raised from $1,000,000 to $10,000,000, and the resulting deferred rent liabilityrequired Minimum Cash Balance (as defined in the Modification Agreement) is $14,138$3,000,000. The Company was in compliance with all of these covenants as of SeptemberJune 30, 2017.

2021. Beginning with the fiscal quarter ending March 31, 2022, the financial covenants return to the original terms specified in the Loan Agreement.

NOTE 8 – INVESTMENT IN EQUITY SECURITIES

The Company’s equity investments consist of non-marketable equity securities in privately held companies without readily determinable fair values, and 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.

17

Table of Contents

The Company made a $500,000 long-term investment in July 2020 to purchase certain non-marketable securities consisting of 7,142,857 Series B-2 Preferred Shares of Direct Dermatology Inc. (“DirectDerm”), representing 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.

On November 9, 2020, the Company entered into agreements to purchase certain non-marketable securities consisting of 150,000 shares of Series A Convertible Preferred Stock (the “Series A Stock”) of Precision Healing Inc. (“Precision Healing”) for an aggregate purchase price of $600,000. The Series A Stock is convertible into 150,000 shares of common stock of Precision Healing and has a senior liquidation preference relative to the common shareholders. This initial investment represented 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 is convertible into 150,000 shares of common stock of Precision Healing. This resulted in ownership of 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. On June 17, 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 to29.0%. For the six months ended June 30, 2021, the Company recorded $278,904 as its share of the loss from equity method investment.

On June 3, 2021, the Company invested $2,084,278 to purchase 278,587 Class A Preferred Shares (the “Shares”) of Pixalere Healthcare, Inc. (“Pixalere”). The Shares are convertible into 28.6% 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 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 Shares in accordance with ASC Topic 323, Investments – Equity Method and Joint Ventures. Due to the substantive liquidation preferences of the Shares over Pixalere’s common stock, the Shares are not “in-substance” common stock, and therefore, the Company will 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 June 30, 2021.

The following summarizes the Company’s investments:

 

 

June 30, 2021

 

 

December 31, 2020

 

 

 

Carrying

Amount

 

 

Economic

Interest

 

 

Carrying

Amount

 

 

Economic

Interest

 

Equity Method Investment

 

 

 

 

 

 

 

 

 

 

 

 

Precision Healing Inc.

 

$1,421,096

 

 

 

29.04%

 

$0

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Cost Method Investments

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Direct Dermatology, Inc.

 

 

500,000

 

 

 

2.9%

 

 

500,000

 

 

 

2.9%

Precision Healing Inc.

 

 

0

 

 

 

 

 

 

 

600,000

 

 

 

12.6%

Pixalere Healthcare, Inc.

 

 

2,084,278

 

 

 

28.6%

 

 

-

 

 

 

 

 

Total Cost Method Investments

 

 

2,584,278

 

 

 

 

 

 

 

1,100,000

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total Investments

 

$4,005,374

 

 

 

 

 

 

$1,100,000

 

 

 

 

 

The following summarizes the loss from the equity method investment reflected in the consolidated statements of operations:

 

 

Three Months ended June 30,

 

 

Six Months Ended June 30,

 

 

 

2021

 

 

2020

 

 

2021

 

 

2020

 

Investment

 

 

 

 

 

 

 

 

 

 

 

 

Precision Healing Inc.

 

$(179,769)

 

$0

 

 

$(278,904)

 

$0

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total

 

$(179,769)

 

$0

 

 

$(278,904)

 

$0

 

18

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NOTE 9 - RELATED PARTIES

Payables to Related Parties

As of September 30, 2017, and December 31, 2016, the

The Company had outstanding payables to related parties totaling $21,842$57,507 at June 30, 2021, and $93,655, respectively. The payables are unsecured, bear no interest223,589 at December 31, 2020.

Manufacturing and due on demand.

Note 5 - Stockholders’ Equity
Preferred Stock
There are currently 5,000,000 shares of Series A Preferred Stock authorized, with no shares of Series A Preferred Stock currently issued or outstanding.
Effective June 24, 2010,Technical Services Agreements – Related Parties

On September 9, 2020, the Company filedexecuted a Certificate of Designations, Number, Voting Power, Preferences and Rights of Series B Convertible Redeemable Preferred Stock (the “Certificate”)manufacturing agreement with Rochal. Under the Texas Secretary of State, designating 7,500 shares of Series B Preferred Stock, par value $10.00 per share (the “Series B Shares”). The Series B Shares rank senior to shares of all other common and preferred stock with respect to dividends, distributions, and payments upon dissolution. Eachterms of the Series B Shares is convertible atmanufacturing agreement, Rochal agreed to manufacture, package, and label products licensed from Rochal by the optionCompany. The manufacturing agreement includes customary terms and conditions for the Company’s industry. The term of the holder into sharesagreement is for a period of common stock as provided infive years unless extended by the Certificate. There are currently no Series B Shares issued or outstanding.

On October 11, 2013,mutual consent of the parties. For the six months ended June 30, 2021, the Company filedincurred no inventory manufacturing costs with Rochal. The Company terminated this agreement on August 12, 2021.

On September 9, 2020, the Company executed a Certificatetechnical services agreement with Rochal. Under the terms of Designations, Number, Voting Power, Preferencesthe technical services agreement, Rochal will provide its expertise and Rights of Series C Convertible Preferred Stock (the “Certificate of Designations”), under which it designated 100,000 shares of Series C Preferred Stock, par value $10.00.services on technical service projects identified by the Company for wound care, skin care and surgical site care applications. The Series C Preferred Stock is entitled to accruing dividends (payable, attechnical services agreement includes customary terms and conditions for the Company’s options, in either cash or stock)industry. For the six months ended June 30, 2021, the Company incurred $234,153 of 5% per annum until October 10, 2016, and 3% per annum until October 10, 2018.

costs for Rochal technical services. The Series C Preferred Stock is seniorCompany terminated this agreement on August 12, 2021.

Rochal Asset Purchase

On July 14, 2021, the Company entered into an asset purchase agreement with Rochal, effective July 1, 2021, pursuant to which the Company’s common stock and any other currently issued seriesCompany agreed to purchased certain assets of the Company’s preferred stock upon liquidation, and is entitled to a liquidation preference per share equal to the original issuanceRochal. The acquired assets were purchased for an aggregate purchase price of such sharesapproximately $1,000,000 consisting of Series C Preferred Stock together with the amount of all accrued but unpaid dividends thereon. Each of the Series C Shares is convertible at the option of the holder into 1,000 shares of common stock as provided(i) approximately $500,000 in the Certificate. Additionally, each holder of Series C Preferred Stock shall be entitled to vote on all matters submitted for a vote of the holders of Common Stock a number of votes equal to the number of full shares of Common Stock into which such holder’s Series C shares could then be converted. As of September 30, 2017,cash and December 31, 2016, there were 85,561 and 85,646 shares of Series C Preferred Stock issued and outstanding, respectively.

On November 13, 2013, the Company filed a Certificate of Designations, Number, Voting Power, Preferences and Rights of Series D Convertible Preferred Stock (the “Certificate of Designations”), under which it designated 25,000 shares of Series D Preferred Stock. Shares of Series D Preferred Stock are not entitled to any preference with respect to dividend or upon liquidation, and will automatically convert (at a ratio of 1,000-to-1) into(ii) 14,369 shares of the Company’s common stock, par value $0.001 upon approvalrepresenting an amount equal to $500,000 based on the average closing sale price of the Company’s stockholders (and filing of) and amendment tocommon stock for the twenty trading days immediately preceding July 14, 2021.

After the asset purchase, Rochal now owns 95,203 shares of the Company’s Certificate of Incorporation increasingcommon stock. Ronald T. Nixon, the number of authorized shares of Common Stock from 100,000,000 to 250,000,000. As of September 30, 2017, and December 31, 2016, there are no shares of Series D Preferred Stock issued and outstanding.


On May 30, 2014, the Company filed a Certificate of Designations, Number, Voting Power, Preferences and Rights of Series E Convertible Preferred Stock (The “Certificate of Designations”), under which it designated 5,000 shares of Series E Preferred Stock. Shares of Series E Preferred Stock are not entitled to any preferenceCompany’s Executive Chairman, is, with respect to dividends orRochal, a director, a significant shareholder indirectly and a majority shareholder with the exercise of certain warrants. Additionally, Ann Beal Salamone, a director of the Company, is a significant shareholder, former president and current Chair of the board of directors of Rochal. See Note 10 for more information regarding this transaction.

NOTE 10 – SUBSEQUENT EVENTS

On July 14, 2021, the Company entered into an asset purchase agreement with Rochal, effective July 1, 2021, pursuant to which the Company agreed to purchase certain assets of Rochal, including, among others, Rochal’s intellectual property, furniture and equipment, supplies, rights and claims, other than certain excluded assets, all as more specifically set forth in the asset purchase agreement, and assume certain liabilities upon liquidation,the terms and will automatically convert (at a ratiosubject to the conditions set forth in the asset purchase agreement. The acquired assets were purchased for an aggregate purchase price of 1,000 sharesapproximately $1,000,000 consisting of Common Stock for every one share of Series E Preferred Stock) into(i) approximately $500,000 in cash and (ii) 14,369 shares of the Company’s common stock, $0.001 par value upon approval ofrepresenting an amount equal to $500,000 based on the Company’s stockholders (and filing of) and amendment to the Company’s Certificate of Incorporation increasing the number of authorized shares of Common Stock from 100,000,000 to 250,000,000. As of September 30, 2017, and December 31, 2016, there are no shares of Series E Preferred Stock issued and outstanding.

On March 7, 2017, the Company issued 715 shares of Series C Preferred Stock for cash proceeds of $50,050.
The Series C preferred stock earned dividends of $100,677 and $213,435 for the nine months ended September 30, 2017 and 2016, respectively. As of September 30, 2017, no Series C preferred stock dividends have been declared.
Common Stock
On March 9, 2017, the Company issued 150,000 shares of common stock to each of the Company’s four Board Directors, (a total of 600,000 shares valued at $42,000).
On March 10, 2017, the Company issued 250,000 shares of common stock valued at $18,250 to a contract consultant upon achievement of specified revenue targets.
On July 31, 2017, the Company issued 937,556 shares of common stock for the conversion of 800 shares of Series C Convertible Preferred Stock and $9,629 of related Series C dividends.
Warrants
During the nine months ended September 30, 2017, 61,326,300 of the 67,246,300 warrants outstanding at the beginning of the period were either forfeited or expired, leaving a balance of 5,920,000 outstanding on September 30, 2017. A summary of the status of the warrants granted for the nine months ended September 30, 2017, and changes during the period then ended is presented below:
 
 
For the Nine Months Ended
September 30, 2017
 
 
 
Shares
 
 
Weighted Average
Exercise Price
 
Outstanding at beginning of period
  67,246,300 
 $0.12 
  Granted
  - 
  - 
  Exercised
  - 
  - 
  Forfeited
  (60,051,300)
  - 
  Expired
  (1,275,000)
    
Outstanding at end of period
  5, 920,000 
 $0.07 
 
 
 
 
  As of September 30, 2017    
 
 
 As of September 30, 2017    
 
 
 
 
 
  Warrants Outstanding    
 
 
 Warrants Exercisable    
 
 
Range of Exercise Prices
 
 
Number Outstanding
 
 
Weighted-Average
Remaining Contract Life
 
 
Weighted- Average
Exercise Price
 
 
Number Exercisable
 
 
Weighted-Average
Exercise Price
 
 $0.06 
  4,500,000 
  1.00 
 $0.06 
  4,500,000 
 $0.06 
  0.08 
  550,000 
  0.43 
  0.08 
  550,000 
  0.08 
  0.09 
  625,000 
  0.54 
  0.09 
  625,000 
  0.09 
  0.15 
  245,000 
  0. 05 
  0.15 
  245,000 
  0.15 
 $0.06 -.15 
  5,920,000 
  .86 
 $0.07 
  5,920,000 
 $0.07 
The aggregate intrinsic value of the exercisable warrants as of September 30, 2017, was $45,000.

On October 10, 2017, Wound Management Technologies, Inc. (the “Company”) and Evolution Venture Partners LLC (“EVP”) entered into a termination agreement (the “Termination Agreement”) terminating, effective as of September 29, 2017, that certain letter agreement dated April 26, 2016, (the “Agreement”), by and between the Company, EVP, and Middlebury Securities, LLC (“Middlebury”). Middlebury terminated its charter on or about July 27, 2016, and therefore is not a party to the Termination Agreement. Pursuant to the Termination Agreement, EVP has agreed to cancel a warrant for the purchase of 60,000,000 sharesaverage closing sale price of the Company’s common stock in exchange for the Company’s issuancetwenty trading days immediately preceding July 14, 2021. The purchase price is subject to EVP of 750,000 shares of Common Stock (the “Shares”). Aspost-closing adjustments pursuant to the fair valueterms of the surrendered warrants exceededasset purchase agreement, which such adjustments must be agreed to by the fair valueparties no later than seventy-five days after the effective date.

Rochal is in the business of creating, developing and commercializing technology innovations in natural and synthetic polymers, antimicrobials and biological systems. As discussed above, the Company previously entered into product license agreements with Rochal, pursuant to which the Company acquired exclusive world-wide licenses to market, sell and further develop certain antimicrobial barrier film and skin protectant products, antimicrobial products for the prevention and treatment of microbes on the human body utilizing certain of Rochal’s patents and a debrider for human medical use to enhance skin condition or treat or relieve skin disorders. Pursuant to the asset purchase agreement, each of the Shares, there is no expense associated with this transaction.

Stock Options
During the nine months ended September 30, 2017, 943,500 of the 1,093,500 options outstanding at the beginning of the period expired. A summary of the status of the stock options granted for the nine-month period ended September 30, 2017,foregoing licenses are being retained by Rochal and changes during the period then ended is presented below:
 
For the Nine Months Ended September 30, 2017
 
 
 
Options
 
 
Weighted Average
Exercise Price
 
Outstanding at beginning of period
  1,093,500 
 $0.15 
Granted
  - 
    
Exercised
  - 
  - 
Forfeited
  - 
  - 
Expired
  (943,500)
 $0.15 
Outstanding at end of period
  150,000 
 
(a)
 
As of September 30, 2017
As of September 30, 2017
Stock Options Outstanding 
Stock Options Exercisable
Exercise Price
Number Outstanding
Weighted-Average
Remaining Contract Life
Weighted- Average
Exercise Price
Number Exercisable
Weighted-Average
Exercise Price
(a)
150,000
-
-
-
  (a) 
(a)
On January 1, 2015, the company granted three tranches of options, 25,000, 25,000, and 100,000 which vest upon meeting specific performance measures agreed upon. The measures include achieving three specific sales targets per month for 3 consecutive months. The exercise price and expiration date of each tranche will be set upon achieving the targets. As of the date of this filing the performance measures have not been met. As a result, the exercise price is undetermined and these options are excluded from the calculation of weighted average remaining life.
The aggregate intrinsic value of the exercisable options as of September 30, 2017 was $0.
Note 6 – Derivative Liabilities
As of December 31, 2013,purchased assets. In addition, the Company did not have a sufficient number of common shares authorized to fulfill the possible exercise of all outstanding warrants and the conversion of all convertible notes payable. As a result, the Company determined that the warrants and the embedded conversion features of the outstanding debt instruments did not qualify for equity classification. Accordingly, the warrants and conversion features were treated as derivative liabilities and were carried at fair value. During the year ended December 31, 2016, all of the outstanding convertible notes that qualified as derivative liabilities were paid in full or converted to common stock. As of September 30, 2017, no warrants remained as derivative liabilities due to their expiration on July 25, 2017.
The following table sets forth the changes in the fair value of derivative liabilities for the nine months ended September 30, 2017:
Balance, December 31, 2016
$(44)
  Gain on change in fair value of derivative liabilities
44
Balance, September 30, 2017
$0
The aggregate gain on derivative liabilities for the nine months ended September 30, 2017 was $44.

Note 7 – Related Party Transactions
On April 25, 2016, the Company and John Siedhoff, a member of the Company’s Board of Directors,previously entered into a Consulting Agreement (the “Agreement”),manufacturing and technical service agreements with Rochal, pursuant to which Mr. Siedhoff providesRochal agreed to manufacture, package and label products the Company licensed from Rochal and provide certain consulting services on technical service projects of the Company.

Pursuant to the Company. The Agreement providedasset 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 paymentmember 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 actually received for any Grant (as defined in the amount of $200,000 to Mr. Siedhoff as compensation for consulting services rendered toasset purchase agreement) by either the Company prioror Rochal. In addition, the Company agreed to April 1, 2016, as well as a consulting feeuse 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 $15,000 per month duringsuch products.

In connection with the termasset purchase agreement, the Company made employment offers to certain employees of Rochal on an “at will” basis, with the Agreement. The Agreement also provides forterms of such employment being consistent with the reimbursement of reasonable and necessary expenses, and may be terminated by either party upon 30 days’ advance written notice. On March 10, 2017,Company’s current employment agreements.

Concurrent with the Agreement, was amended to: (i) change the name of the consultant under the Agreement from John Siedhoff to Twin Oaks Equity, LLC (an entity controlled by Mr. Siedhoff), and (ii) increase the monthly compensation payable from $15,000 to $20,000, effective as of January 1, 2017. The consulting fee expense was $220,000 for the nine months ended September 30, 2017, (including a bonus of $40,000 in recognition of 2016 results).

Note 8 – Capital Lease Obligation
In December 2014,asset purchase, on July 14, 2021, the Company entered into a Capital Leaseconsulting agreement with Ms. Salamone pursuant to which Ms. Salamone will 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 purchaseconsulting services to be provided to the Company, Ms. Salamone is entitled to receive an annual consulting fee of a phone system.$177,697, with payments to be paid once per month. The consulting agreement required a down paymenthas an initial term of $2,105 and 36 monthly payments of $375. The Company recorded an asset of $13,512 and a capital lease obligation of $13,512. Aggregate payments under the lease were $3,423 for the nine months ended September 30, 2017. At September 30, 2017, a total lease liability of $344 remained which is due in full in 2017.
Note 9 – Subsequent Events
On November 1, 2017,three years, unless earlier terminated by the Company, and Ken Link entered into a binding settlementis subject to renewal. The consulting agreement which will result in dismissal with prejudice of all claimsalso contains customary provisions related to, among other things, confidentiality, and counterclaims asserted in Cause No. 342-256486-11, in exchangetermination for which the Company will deliver to Ken Link 1,200,000 shares of Wound Management Technologies, Inc. common stock in total satisfaction of all obligations between the parties. As a result of this settlement the Note Payable to Mr. Link in the amount of $223,500 is cancelled.

Itemcause provisions.

19

Table of Contents

ITEM 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

The following discussion of ourthe financial condition and results of operations of Sanara MedTech Inc. (collectively with its consolidated subsidiaries, the “Company,” “Sanara MedTech,” “Sanara,” “SMTI,” “we,” “our,” or “us”) 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, 20162020 and with the unaudited consolidated financial statements and related notes thereto presented in this Quarterly Report on Form 10-Q.

Forward-Looking Statements

Some

This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). These statements contained in this reportmay discuss expectations as to future expectations, contain projections oftrends, plans, events, results of operations or financial condition, or state other "forward-looking" information. Theinformation relating to the Company, including, without limitation, statements concerning the impact of the COVID-19 pandemic and our expectations for SG&A expense. Statements, other than statements of historical fact, included in this Quarterly Report on Form 10-Q are forward-looking statements and generally may be identified by words "believe," "intend," "plan," "expect," "anticipate," "estimate," "project," "goal" andsuch as “anticipate,” “believe,” “continue,” “contemplate,” “could,” “estimate,” “expect,” “forecast,” “guidance,” “intend,” “may,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would” or other similar expressions identify such a statement was made.words, phrases or expressions. These statements should be viewed with caution and are subject to knownvarious risks and unknown risks, uncertainties, many of which are outside of the Company’s control. The following factors, among others, could cause actual results to differ materially from those in the forward-looking statements:

·

unanticipated changes in the markets for the Company’s business;

·

unanticipated downturns in business relationships with customers or their purchases from us;

·

the potential effects on our businesses from natural disasters;

·

the availability of credit to customers and suppliers;

·

competitive pressures on sales and pricing;

·

unanticipated changes in the cost of inventory and other operating costs;

·

the introduction of competing products;

·

unexpected technical or marketing difficulties; unexpected claims, charges, litigation or dispute resolutions;

·

new laws and governmental regulations; stock market and currency fluctuations;

·

war, civil or political unrest or terrorism;

·

the course of the COVID-19 pandemic and government responses thereto; and

·

unanticipated deterioration of economic and financial conditions in the United States and around the world.

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 contemplated by the statements. Theanticipated in these forward-looking information is based on various factors and is derived using numerous assumptions. Factors that might cause or contribute to such a discrepancy include, but are not limited to the risks discussedstatements, see “Risk Factors” in this and our other SEC filings. We do not promise to update forward-looking information to reflect actual results or changes in assumptions or other factors that could affect those statements. Future events and actual results could differ materially from those expressed in, contemplated by, or underlying such forward-looking statements.

The following discussion and analysisPart I, Item 1A of our financial condition is as of September 30, 2017.  Our results of operations and cash flows should be read in conjunction with our unaudited financial statements and notes thereto included elsewhere in this report and the audited financial statements and the notes thereto included in our Form 10-K for the year ended December 31, 2016.
Business Overview
Unless otherwise indicated, we use “WMT,” “the Company,” “we,” “our” and “us” in this report to refer to the businesses of Wound Management Technologies, Inc.
Wound Management Technologies, Inc. (“WMT” or the “Company”) was organized on December 14, 2001, as a Texas corporation under the name eAppliance Innovations, Inc. In June of 2002, MB Software Corporation, a public corporation formed under the laws of Colorado, merged with the Company (which at the time was a wholly owned subsidiary of MB Software Corporation), and the Company changed its name to MB Software Corporation as part of the merger. In May of 2008, the Company changed its name to Wound Management Technologies, Inc.
The Company, through its wholly-owned subsidiary, Wound Care Innovations, LLC (WCI), markets and sells the patented CellerateRX® Activated Collagen® products in the expanding advanced wound care market. CellerateRX’s activated collagen, which is approximately 1/100th the size of native collagen, delivers the essential benefits of collagen to a wound immediately—other forms of native, intact collagen in commercially available products require time for the body to prepare the collagen for use in the wound healing process. CellerateRX is cleared by the FDA as a medical device for use on all acute and chronic wounds, except third degree burns, and are offered in both gel and powder form. CellerateRX is currently approved for reimbursement under Medicare Part B and no prescription is required.
We believe that these products are unique in composition, applicability and clinical performance, and demonstrate the ability to reduce costs associated with standard wound management. The Company is focused on delivering the CellerateRX® product line to hospitals and surgery centers as well as the diabetic care and long-term care markets.
Resorbable Orthopedic Products, LLC (“ROP”) a wholly-owned subsidiary of the Company was organized as a Texas limited liability company on August 24, 2009, as part of a transaction to acquire a multi-faceted patent for resorbable bone hemostasis products. ROP is both licensing technology from this patent and also developing products itself. In 2014, the Company entered into a commercial license for a bone void filler. The Company began receiving royalties under this agreement in the fourth quarter of 2013. Royalties will continue for the life of the patent which expires in 2023. In 2016 ROP received FDA 510(k) clearance for HemaQuell™ Resorbable Bone Hemostat. HemaQuell™ is a mechanical tamponade for bleeding bone that resorbs within 2-7 days after use. In the first quarter of 2017, ROP launched HemaQuell® Resorbable Bone Hemostat via the Company’s Innovate OR, Inc, subsidiary. Initial sales efforts are focused on orthopedic, cardiovascular, and spine surgeries.
Our primary focus is developing and marketing products for the advanced wound care market, with a focus on surgical products, as pursued through our wholly owned subsidiaries, WCI and ROP, which brings a unique mix of products, procedures and expertise to the wound care arena including surgical wounds. CellerateRX’s patented Activated Collagen fragments (CRa® are a fraction of the size of the native collagen molecules and particles found in other products, which delivers the benefits of collagen to the body immediately.

Management Letter
Wound Management Technologies, Inc. is pleased to report revenues of $1,549,016 for the third quarter of 2017, an increase of approximately 10% over the $1,409,530 reported during the same period in 2016. Year-to-date revenues of $4,607,162 for the nine months ended September 30, 2017, were up 22% from the $3,762,681 reported during the same period in 2016. This increase of approximately $845,000 is the result of continued expansion of our network of distributor sales partners since the third quarter of 2016. Although third quarter revenues were up from the previous quarter by approximately $100,000, revenues from the Texas Coast were down approximately $65,000 from the previous quarter primarily during a period in which the region was feeling the impact of Hurricane Harvey.
Although we incurred a net loss of $48,562 for the three-months ended September 30, 2017, year-to-date remained profitable with net income of $83,539 for the nine-months ended September 30, 2017. The current quarter loss was primarily due to sales and marketing initiatives including HemaQuell™ prelaunch expenses, and sales advisory services. Additional one-time consulting expenses were incurred related to a new business development opportunity that we decided not to pursue.
 In the first nine-months of this year we completed another three-year Strategic Plan initiative by retiring all amortized notes payable.
We are continuing to focus on growing CellerateRX® revenues by developing and carrying out our strategic initiatives to: grow our sales force; expand our surgical product sales to new customers; and increase sales to existing customers. Our Regional Sales Managers are working closely with our distributor and representative network to increase awareness and sales. We are also increasing our market presence with continuing case studies by key opinion leaders.
The Company hired a seasoned medical industry veteran with experience in both surgical suite sales and general wound care as Director of Strategic Accounts in September of this year, to spearhead our efforts to expand our distributor partner networks and to work with strategic partners to facilitate the product’s adoption by major hospital systems across the Country.
In closing, Wound Management Technologies continues to be well positioned to execute our strategic growth initiatives with a solid go-to-market plan in place.  The Company looks forward to capitalizing on the traction it has built in the market thus far with additional investments in strategic growth, sales, marketing and clinical support for CellerateRX® and HemaQuell™.
Results of Operations
For the three and nine months ended September 30, 2017, compared with the three and nine months ended September 30, 2016:
Revenues.  The Company generated revenues of $1,549,016 for the three months ended September 30, 2017, compared to revenues of $1,409,530 for the three months ended September 30, 2016, representing a 10% increase in revenues. The Company generated revenues for the nine months ended September 30, 2017, of $4,607,162, compared to revenues of $3,762,681 for the nine months ended September 30, 2016, or a 22% increase in revenues. The increase in revenues is the result of an expanded salesforce and the successful implementation of the Company’s strategic plan to introduce our products into hospital operating rooms and surgery centers. Revenues include $50,250 in royalty income for each of the three months ended September 30, 2017 and 2016, and $150,750 in royalty income for each of the nine months ended September 30, 2017 and 2016 from the development and license agreement the Resorbable Orthopedic Products, LLC subsidiary (ROP) executed with BioStructures, LLC in 2011.
Cost of goods sold. Cost of goods sold for the three months ended September 30, 2017, was $230,049, compared to costs of goods sold of $211,639 for the three months ended September 30, 2016, (a 9% increase). Cost of goods sold for the nine months ended September 30, 2017, was $568,071, as compared to costs of goods sold of $612,514 for the nine months ended September 30, 2016, (a 7% decrease). Although revenues increased by 22% over the nine-month period, cost of goods sold as a percent of revenues decreased as a result of the increase in the percent of surgical sales which have a greater gross profit margin.
Selling, generalandadministrativeexpenses(“SG&A"). SG&A expenses for the three months ended September 30, 2017, were $1,303,344, as compared to SG&A expenses of $963,738 for the three months ended September 30, 2016, a 35% increase in SG&A expenses. SG&A expenses for the nine months ended September 30, 2017, were $3,799,644, as compared to SG&A expenses of $2,827,340 for the nine months ended September 30, 2016, or a 34% increase in SG&A expenses. SG&A expenses increased primarily due to sales commission expense related to the revenue increase, payroll expenses as we grow our infrastructure and consulting fees related to strategic initiatives.
Other administrative expense. Other administrative expenses for the nine months ended September 30, 2016, consisted of a onetime non-cash expense of $758,665 for a warrant to purchase shares of the Company’s stock and a onetime cash expense of $60,000 for professional fees, both incurred in the Second Quarter related to a strategic growth initiative.

Interest expense. Interest expense was $19,807 for the three months ended September 30, 2017, as compared to $42,433 for the three months ended September 30, 2016. Interest expense was $115,421 for the nine months ended September 30, 2017, as compared to $132,689 for the nine months ended September 30, 2016. This change was due to amending several notes and recapturing previous expensed interest expense.
Net income/loss. We had a net loss of $48,562 for the three months ended September 30, 2017, compared to net income of $181,487 for the three months ended September 30, 2016. The current quarter loss was primarily due to sales and marketing initiatives including HemaQuell™ prelaunch expenses, a National Sales Meeting, and sales advisory services. Additional one-time consulting expenses were incurred related to a new business development opportunity that we decided not to pursue. We had net income of $83,539 for the nine months ended September 30, 2017, compared to a net loss of $650,675 for the nine months ended September 30, 2016. The 2016 loss was primarily due to a onetime non-cash expense of $758,665 for a warrant to purchase shares of the Company’s stock and a onetime cash expense of $60,000 for professional fees, both incurred in the Second Quarter related to a strategic growth initiative.
Liquidity and Capital Resources
As a result of the current status of the Company’s two Convertible notes payable to Related parties totaling $1,200,000, the Company has a working capital deficit of $448,630 as of September 30, 2017, a decrease of $1,050,284 from the 2016 year-end surplus balance of $601,654.
As of September 30, 2017, we had total current assets of $1,888,182, including cash of $151,314 and inventories of $820,908. As of December 31, 2016, our current assets of $1,996,013 included cash of $833,480 and inventories of $348,457.
As of September 30, 2017, we had total current liabilities of $2,336,812 including $223,500 of notes payable. Our current liabilities also include $232,511 of current year royalties payable. As of December 31, 2016, our current liabilities of $1,394,359 included $414,338 of notes payable and prior year accrued royalties payable of $276,916.
As of September 30, 2017, no derivative liabilities remained due to the expiration of the related warrants on July 25, 2017. At December 31, 2016, our derivative liabilities totaled $44 related to 10,000 of the 21,736,844 outstanding stock purchase warrants.
For the nine months ended September 30, 2017, net cash used in operating activities was $411,503 compared to $10,091 used in the first nine months of 2016.
In the nine months ended September 30, 2017, net cash used in investing activities was $126,453 compared to $3,029 used in the first nine months of 2016.
In the nine months ended September 30, 2017, net cash used in financing activities was $144,210. For the nine months ended September 30, 2016, financing activities provided $273,743.
Off-Balance Sheet Arrangements
None.
Recent Accounting Pronouncements
For the period ended September 30, 2017, there were no other changes to our critical accounting policies as identified in our Annual Report on Form 10-K for the year ended December 31, 2016.
In May 2014,2020, Part II, Item 1A, “Risk Factors” and elsewhere in this Quarterly Report on Form 10-Q. Forward-looking statements speak only as of the Financial Accounting Standards Board (FASB) issued Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customersdate on which they are made, and the Company does not assume any obligation to update these forward-looking statements.

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 and chronic wound and skin care markets. Our portfolio of products and services is designed to allow us to deliver comprehensive wound and skin care solutions for patients in all care settings, including acute (hospitals and long-term acute care hospitals (“LTACHs”)) and post-acute (wound care clinics, physician offices, skilled nursing facilities (“SNFs”), home health, hospice, and retail). 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 wound and skin care products and technologies and are continually seeking to expand our offerings for reporting periodspatients requiring wound and skin care treatments across the entire continuum of care in the United States.

We currently market seven products across chronic and surgical wound care applications and have multiple products in our pipeline. We license our products from research and development partners Applied Nutritionals, LLC (“AN”) (through a sublicense with CGI Cellerate RX, LLC (“CGI Cellerate RX”), an affiliate of The Catalyst Group, Inc. (“Catalyst”)) and Rochal Industries, LLC (“Rochal”) and have the right to exclusively distribute certain products under development by Cook Biotech Inc. (“Cook Biotech”). In 2021, we intend to begin marketing two biologic products for surgical and wound care applications pursuant to our marketing and distribution agreement with Cook Biotech.

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In June 2020, we formed a subsidiary, United Wound and Skin Solutions LLC (“UWSS”), to hold certain investments and operations in wound and skin care virtual consult services. We anticipate that our various service offerings will allow clinicians/physicians utilizing our technologies to collect and analyze large amounts of data on patient conditions and outcomes that will improve treatment protocols and ultimately lead to more evidence-based formulary to improve patient outcomes. We intend to launch our initial virtual consult service offerings in late 2021. Through a combination of our UWSS services and our Sanara products, we believe we will be able to offer patient care solutions at every step in the continuum of wound and skin care from diagnosis through healing.

Effective July 1, 2021, we acquired certain assets from Rochal, including, among others, intellectual property, four 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.

Impact of the COVID-19 Pandemic

Beginning in March 2020, many states issued orders suspending elective surgeries in order to free-up hospital resources to treat COVID-19 patients. This resulted in a reduction in demand for our surgical products beginning in the second half of March 2020. Additionally, most states limited access to SNFs to only resident caregivers, which impeded our ability to provide education and product training to the clinicians who use our products in these facilities. These restrictions resulted in an overall decline in sales for the second quarter of 2020. During the second half of 2020 and the first quarter of 2021, we saw a strong rebound in product sales as restrictions on elective surgeries eased in our primary markets in Texas, Florida, and the southeastern United States.

Due to recent COVID-19 resurgences and variants, the duration and effects of the pandemic remain uncertain; however, management believes that elective surgical procedures will continue to be performed with the exception of certain geographic hotspots. We will continue to closely monitor the pandemic in order to ensure the safety of our people and our ability to serve our customers and patients.

Recent Developments

February 2021 Offering

On February 12, 2021, we entered into an underwriting agreement (the “Underwriting Agreement”) with Cantor Fitzgerald & Co. as representative of several underwriters named therein (collectively, the “Underwriters”), pursuant to which we agreed to issue and sell an aggregate of 1,100,000 shares of our common stock to the Underwriters at a price to the public of $25.00 per share, less underwriting discounts and commissions (the “Offering”). Pursuant to the Underwriting Agreement, the Company granted the Underwriters a 30-day option to purchase up to an additional 165,000 shares of common stock at the public offering price, less underwriting discounts and commissions, which the Underwriters exercised in full. The Offering, including the purchase of the 165,000 additional shares of common stock, closed on February 17, 2021.

The net proceeds to us from the Offering were $28.9 million, after (i) giving effect to the Underwriter’s full exercise of its option to purchase additional shares of common stock, and (ii) deducting the underwriting discounts and commissions and offering expenses payable by us.

Pixalere Investment

On June 3, 2021, we invested $2,084,278 to purchase 278,587 Class A Preferred Shares (the “Shares”) of Pixalere Healthcare, Inc. (“Pixalere”). The Shares are convertible into 28.6% 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 our purchase of the Shares, Pixalere granted Pixalere Healthcare USA, LLC (“Pixalere USA”), our subsidiary, a royalty-free exclusive license to use the Pixalere software and platform in the United States. In conjunction with the grant of the license, we issued Pixalere a 27.3% equity ownership interest in Pixalere USA valued at $93,879.

Rochal Asset Purchase and Consulting Agreement

On July 14, 2021, we entered into an asset purchase agreement with Rochal, effective July 1, 2021, pursuant to which we agreed to purchase certain assets of Rochal, including, among others, Rochal’s intellectual property, furniture and equipment, supplies, rights and claims, other than certain excluded assets, all as more specifically set forth in the asset purchase agreement, and assume certain liabilities upon the terms and subject to the conditions set forth in the asset purchase agreement. The acquired assets were purchased for an aggregate purchase price of approximately $1,000,000 consisting of (i) approximately $500,000 in cash and (ii) 14,369 shares of our common stock, representing an amount equal to $500,000 based on the average closing sale price of our common stock for the twenty trading days immediately preceding July 14, 2021. The purchase price is subject to post-closing adjustments pursuant to the terms of the asset purchase agreement, which such adjustments must be agreed to by the parties no later than seventy-five days after the effective date. We believe that by acquiring these assets, we will incur approximately $1.2 million to $1.5 million in additional operating expenses in the first 12 months following the acquisition, but some of this expense could be offset by future grants and outside contract revenue that may be received by us as a result of the acquisition.

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Rochal is in the business of creating, developing and commercializing technology innovations in natural and synthetic polymers, antimicrobials and biological systems. Prior to the asset purchase, we previously entered into product license agreements with Rochal, pursuant to which the Company acquired exclusive world-wide licenses to market, sell and further develop certain antimicrobial barrier film and skin protectant products, antimicrobial products for the prevention and treatment of microbes on the human body utilizing certain of Rochal’s patents and a debrider for human medical use to enhance skin condition or treat or relieve skin disorders. Pursuant to the asset purchase agreement, each of the foregoing licenses are being retained by Rochal and are excluded from the purchased assets. In addition, we previously entered into manufacturing and technical service agreements with Rochal, pursuant to which Rochal agreed to manufacture, package and label products we licensed from Rochal and provide certain services on technical service projects for us. On August 12, 2021, we terminated each of the manufacturing and technical services agreements with 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 actually received for any Grant (as defined in the asset purchase agreement) by either us or Rochal. In addition, we 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 us to intellectual property rights from Rochal in respect of such products.

In connection with asset purchase agreement, we made employment offers to certain employees of Rochal on an “at will” basis, with the terms of such employment being consistent with our current employment agreements.

Concurrent with the asset purchase, on July 14, 2021, we entered into a consulting agreement with Ms. Salamone pursuant to which Ms. Salamone will 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. The consulting agreement also contains customary provisions related to, among other things, confidentiality, and termination for cause provisions.

Components of Results of Operations

Sources of Revenues

Our revenue is derived primarily from sales of our surgical products to hospitals and other acute care facilities, and sales of our chronic wound care products to customers across the post-acute continuum of care. 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 our product is received by the customer.

Revenue streams from product sales and royalties are summarized below for the six months ended June 30, 2021 and June 30, 2020. All revenue was generated in the United States.

 

 

Six Months Ended

 

 

 

June 30,

 

 

 

2021

 

 

2020

 

Surgical

 

$10,732,431

 

 

$6,000,376

 

Wound Care

 

 

453,638

 

 

 

390,638

 

Royalty revenue

 

 

100,500

 

 

 

100,500

 

Total Revenue

 

$11,286,569

 

 

$6,491,514

 

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 throughout the life of the patent which expires in 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 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 revenue less the cost of goods sold, and gross margin is gross profit expressed as a percentage of total revenue.

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Operating Expenses

Selling, general and administrative expenses (“SG&A”) consist primarily of salaries, sales commissions, benefits, bonuses, and stock-based compensation. SG&A also includes outside legal counsel, audit fees, insurance premiums, rent, and other corporate expenses. We expense all SG&A expenses as incurred.

Research and development expenses (“R&D”) include costs related to enhancements to our currently available products and additional investments in our product and platform development pipeline. We expense research and development costs as incurred. We generally expect that R&D expenses will increase as we continue to support product enhancements as well as to bring new products to market.

Other Income (Expense)

Other income (expense) is primarily comprised of gains or losses on equity method investments, interest income, interest expense and other non-operating activities.

Results of Operations

Revenues. For the three months ended June 30, 2021, we generated revenues of $6,277,133 compared to revenues of $2,967,183 for the three months ended June 30, 2020, representing a 112% increase from the prior year period. For the six months ended June 30, 2021, revenues totaled $11,286,569 compared to revenues of $6,491,514 for the six months ended June 30, 2020, representing a 74% increase from the prior year period. The higher revenues in 2021 were primarily due to increased sales of surgical wound care products as a result of our sales force expansion last year and our continuing strategy to expand our independent distribution network in both new and existing U.S. markets. In addition, revenues in the second quarter of 2020 were negatively impacted due to the suspension of elective surgeries and restricted access to patient facilities throughout most parts of the United States as a result of the COVID-19 pandemic.

Cost of goods sold. Cost of goods sold for the three months ended June 30, 2021, was $536,405, compared to Cost of goods sold of $348,675 for the three months ended June 30, 2020. Cost of goods sold for the six months ended June 30, 2021 was $1,010,838, compared to Cost of goods sold of $678,863 for the six months ended June 30, 2020. The increase over the prior year period was primarily due to higher sales volume.

Selling, generalandadministrativeexpenses. SG&A expenses for the three months ended June 30, 2021, were $6,562,144, as compared to $3,582,511 for the three months ended June 30, 2020. SG&A expenses for the six months ended June 30, 2021, were $11,971,874 compared to SG&A expenses of $8,514,662 for the six months ended June 30, 2020. The higher SG&A expenses in 2021 were primarily due to increased payroll costs resulting from sales force expansion and operational support, and higher sales commission expense as a result of higher product sales. As part of our strategy to expand our sales reach in new and existing markets, we employed eight additional field sales managers during the first half of 2021. As of June 30, 2021, we had a total of 26 field sales managers.

Research and developmentexpenses. R&D expenses for the three months ended June 30, 2021, were $103,981 compared to $41,516 for the three months ended June 30, 2020. R&D expenses for the six months ended June 30, 2021, were $222,193 compared to $45,903 for the six months ended June 30, 2020. The higher R&D expenses in 2021 were primarily due to the initiation of new studies and development projects for currently licensed products.

Other expense. Other expense for the three months ended June 30, 2021, was $179,769 compared to $49,817 for the three months ended June 30, 2020. Other expense for the six months ended June 30, 2021 was $279,615 compared to $94,929 for the six months ended June 30, 2020. The higher Other expense in 2021 was due to the recognition of a non-cash loss of $278,904 from our equity method investment in Precision Healing. Interest expense was $711 for the six months ended June 30, 2021, as compared to $9,455 for the six months ended June 30, 2020. The higher Interest expense in 2020 was due to interest expense associated with our unsecured promissory note under the Paycheck Protection Program, and interest on a convertible promissory note which was converted to common stock in early 2020.

Net income / loss. We had a net loss of $1,205,973 for the three months ended June 30, 2021, compared to net loss of $1,129,557 for the three months ended June 30, 2020. For the six months ended June 30, 2021, we had a net loss of $2,389,349, compared to net loss of $2,970,569 for the six months ended June 30, 2020. The improvement in our net loss for the six months ended June 30, 2021 was primarily due to higher sales revenues in 2021 compared to the same period in 2020.

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Liquidity and Capital Resources

Cash on hand at June 30, 2021 was $24,389,004, compared to $455,366 at December 31, 2020.  Historically, we have financed our operations primarily from the sale of equity securities.  In 2020, our principal sources of liquidity were cash generated from operations, availability of our bank line of credit, and cash provided by an unsecured promissory note in the principal amount of $583,000 (“the PPP Loan”) to Cadence Bank, N.A. (“Cadence”).  On February 12, 2021, we closed an underwritten public offering of 1,265,000 shares of our common stock at a public offering price of $25.00 per share resulting in gross proceeds of $31,625,000, before deducting underwriting discounts and commissions and offering expenses. We expect to use the net proceeds from the offering to expand our salesforce and for further development of our products, services and technologies pipeline, clinical studies and general corporate purposes, including working capital and acquisitions. Based on our current plan of operations, including acquisitions, we believe our cash on hand, when combined with expected cash flows from operations and amounts available under our revolving credit facility, 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.

On January 15, 2017.2021, we entered into a new loan agreement with Cadence (the “Loan Agreement”), providing for a $2.5 million revolving line of credit. The revolving line of credit matures on January 13, 2023 and is secured by substantially all of our assets. Any amounts outstanding will bear interest of 0.75% plus the “Prime Rate” designated in the “Money Rates” section of the Wall Street Journal. Proceeds from the line of credit are to be used to provide additional working capital in support of current assets and for other general corporate purposes and may not be used for acquisitions.

The line of credit contains customary representations and warranties and requires us to maintain compliance with certain financial covenants, including, among others, a minimum liquidity of $1,000,000 as of December 31, 2020 and March 31, 2021, a minimum Tangible Net Worth (as defined in the Loan Agreement) of $1,000,000 and, beginning with the fiscal quarter ending June 30, 2021, a minimum Interest Coverage Ratio (as defined in the Loan Agreement) of 1.5 to 1.0. The Loan Agreement also contains customary events of default. If such an event of default occurs, Cadence would be entitled to take various actions, including the acceleration of amounts due under the Loan Agreement. We generally may (and must, under certain circumstances) prepay all or a portion of the principal outstanding on the revolving line of credit prior to its contractual maturity. On February 11, 2021, we made an $800,000 draw on the revolving line of credit. On February 19, 2021, we paid down the entire balance of the revolving line of credit. As of June 30, 2021, no amounts were owed under the Loan Agreement.

On June 29, 2021, we amended the revolving line of credit with Cadence to modify certain financial covenants which included changing the initial measurement period of the minimum Interest Coverage Ratio (as defined in the Loan Agreement) from June 2021 to March 2022 (the “Modification Agreement”).  In connection with this change, beginning with the fiscal quarter ended June 30, 2021 through the fiscal quarter ending December 31, 2021, the required minimum Tangible Net Worth (as defined in the Loan Agreement) was raised from $1,000,000 to $10,000,000, and the required Minimum Cash Balance (as defined in the Modification Agreement) is $3,000,000. The Company has reviewedwas in compliance with all of these covenants as of June 30, 2021. Beginning with the pronouncementfiscal quarter ending March 31, 2022, the financial covenants return to the original terms specified in the Loan Agreement.

On November 9, 2020, our subsidiary, UWSS, entered into agreements to purchase shares of Series A Convertible Preferred Stock (the “Series A Stock”) of Precision Healing Inc. (“Precision Healing”) for an aggregate purchase price of $600,000. UWSS made additional investments of $600,000 in February 2021 and believes it$500,000 in June 2021 for 275,000 additional shares of Series A Stock.

On July 7, 2019, we executed a license agreement with Rochal whereby we 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”). Under the terms of the BIAKŌS License Agreement, we agreed to pay Rochal $750,000 upon the completion of a capital raise, on or before December 31, 2022, of at least $10,000,000 through the sale of our common stock or assets. At our option, the $750,000 payment may be paid in any combination of cash and our common stock. In March 2021, we issued 20,834 shares of our common stock to Rochal as full payment of the $750,000 which became due upon the Company’s completion of a capital raise in February 2021.

On June 3, 2021, we invested $2,084,278 for 278,587 Class A Preferred Shares (the “Shares”) of Canada based Pixalere Healthcare, Inc. (“Pixalere”). The Shares are convertible into 28.6% 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 our purchase of the Shares, Pixalere granted Pixalere Healthcare USA, LLC (“Pixalere USA”), our subsidiary, a royalty-free exclusive license to use the Pixalere software and platform in the United States. In conjunction with the grant of the license, we issued Pixalere a 27.3% equity ownership interest in Pixalere USA valued at $93,879.

Effective July 1, 2021, we acquired certain assets from Rochal. The acquired assets were purchased for an aggregate purchase price of approximately $1,000,000 consisting of (i) approximately $500,000 in cash and (ii) 14,369 shares of our common stock, representing an amount equal to $500,000 based on the average closing sale price of our common stock for the twenty trading days immediately preceding July 14, 2021. The purchase price is subject to post-closing adjustments pursuant to the terms of the asset purchase agreement, which such adjustments must be agreed to by the parties no later than seventy-five days after the effective date.

Cash Flow Analysis

For the six months ended June 30, 2021, net cash used in operating activities was $1,595,895 compared to $2,732,191 used in operating activities for the six months ended June 30, 2020. The lower use of cash in 2021 was primarily due to higher sales revenue.

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For the six months ended June 30, 2021, net cash used in investing activities was $3,209,724 compared to $1,157,456 used in investing activities during the six months ended June 30, 2020. The increase in cash used in investing activities in 2021 was due to the purchase of 275,000 additional shares of Series A Stock of Precision Healing for $1,100,000, and the purchase of 278,587 Shares of Pixalere for $2,084,278. The cash used in investing activities in 2020 was due to a $500,000 milestone payment made to Rochal as a result of FDA clearance of BIAKŌS Antimicrobial Wound Gel and a $600,000 initial payment upon acquisition of the debrider product license agreement from Rochal.

For the six months ended June 30, 2021, net cash provided by financing activities was $28,739,257 as compared to $583,000 provided by financing activities for the six months ended June 30, 2020. The cash provided by financing activities in 2021 was due to proceeds received pursuant to an underwritten public offering of 1,265,000 shares of our common stock at a public offering price of $25.00 per share resulting in gross proceeds of $31,625,000, before deducting underwriting discounts and commissions and offering expenses.

Material Transactions with Related Parties

CellerateRX Sublicense Agreement

We have an exclusive, world-wide sublicense to distribute CellerateRX products into the wound care and surgical markets from an affiliate of Catalyst, CGI Cellerate RX, LLC (“CGI Cellerate RX”), which licenses the rights to CellerateRX from Applied Nutritionals. Sales of CellerateRX have comprised the majority of our sales during 2018, 2019 and 2020. On January 26, 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 CellerateRX exceed $1,000,000. We pay royalties based on our annual Net Sales of CellerateRX (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. Minimum royalties of $400,000 per year are payable for the first five years of the sublicense agreement, which was entered on August 27, 2018. For the six months ended June 30, 2021 and 2020, royalties accrued under the terms of this agreement totaled $404,220 and $210,220, respectively.

Ronald T. Nixon, our Executive Chairman, is the founder and managing partner of Catalyst. Mr. Nixon and Catalyst, collectively with their affiliates, including CGI Cellerate RX, beneficially owned 3,502,240 shares of our common stock as of June 30, 2021.

Convertible Notes Payable

On March 15, 2019, we acquired Catalyst’s 50% interest in Cellerate, LLC in exchange for the issuance of 1,136,815 shares of our newly created Series F Convertible Preferred Stock (the “Cellerate Acquisition”). In connection with the Cellerate Acquisition, we issued a 30-month convertible promissory note to CGI Cellerate RX, an affiliate of Catalyst, in the principal amount of $1,500,000, bearing interest at a 5% annual interest rate, compounded quarterly. Interest on the promissory note was payable quarterly but could have been deferred at our election to the maturity of the promissory note. Outstanding principal and interest were convertible at CGI Cellerate RX’s option into shares of our common stock at a conversion price of $9.00 per share.

On February 7, 2020, CGI Cellerate RX converted its $1,500,000 promissory note, including accrued interest of $111,911, into 179,101 shares of our common stock. CGI Cellerate RX also converted its 1,136,815 shares of Series F Convertible Preferred Stock into shares of the Company’s common stock. For more information, see Note 6 to the unaudited consolidated financial statements contained in this Quarterly Report on Form 10-Q. As of June 30, 2021, there were no related party promissory notes or accrued interest outstanding.

Manufacturing and Technical Services Agreements

On September 9, 2020, we executed a manufacturing agreement with Rochal. Under the terms of the manufacturing agreement, Rochal agreed to manufacture, package, and label products we licensed from Rochal. The manufacturing agreement includes customary terms and conditions. The term of the agreement is for a period of five years unless extended by the mutual consent of the parties. For the six months ended June 30, 2021, we incurred no inventory manufacturing costs with Rochal.  The Company terminated this agreement on August 12, 2021.

On September 9, 2020, we executed a technical services agreement with Rochal. Under the terms of the technical services agreement, Rochal will provide its expertise and services on technical service projects identified by us for wound care, skin care and surgical site care applications. The technical services agreement includes customary terms and conditions for our industry. For the six months ended June 30, 2021, we incurred $234,153 of costs for Rochal technical services. The Company terminated this agreement on August 12, 2021.

Ronald T. Nixon, our Executive Chairman, is also a director of Rochal, and indirectly a significant shareholder of Rochal, and through the potential exercise of warrants a majority shareholder of Rochal. Ann Beal Salamone, a director, is a significant shareholder and current Chairman of the Board of Rochal.

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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 Policies

Our discussion and analysis of our financial condition and results of operations are based on our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the Company’sU.S. The preparation of these consolidated financial position, operations or cash flows.

In February 2016,statements requires us to make estimates and judgments that affect the FASB issued ASC 842 Leases which isreported amounts of assets, liabilities, and expenses.

We base our estimates on historical experience and on various other assumptions that we believe to be effectivereasonable under the circumstances. The results of these assumptions form the basis for reporting periods beginning after December 15, 2018. The Companymaking judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Under different assumptions or conditions, actual results may differ from these estimates. We have identified certain significant accounting policies which involve a higher degree of judgment and complexity in making certain estimates and assumptions that affect amounts reported in our consolidated financial statements, as summarized below.

Revenue Recognition

We recognize revenue in accordance with Accounting Standards Codification (“ASC”) Topic 606, Revenue from Contracts with Customers, which we adopted on January 1, 2018 using the modified retrospective method. Revenues are recognized when control of the promised goods or services is currently reviewing any impacttransferred to the customer in an amount that it will havereflects the consideration we expect to be entitled to receive in exchange for transferring those goods or services. Revenue is recognized based on the Company’sfollowing 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, we satisfy a performance obligation

Impairment of Long-Lived Assets

Long-lived assets, including certain identifiable intangibles held and to be used by our Company, are reviewed for impairment whenever events or changes in circumstances, including the COVID-19 pandemic, indicate that the carrying amount of such assets may not be recoverable. We continuously evaluate the recoverability of our long-lived assets based on estimated future cash flows and the estimated liquidation value of such long-lived assets and provide 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 net realizable value. No impairment was recorded during the six months ended June 30, 2021 and 2020.

Investment in Equity Securities

Our investments consist of non-marketable equity securities in privately held companies without readily determinable fair values, and 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. We have reviewed the carrying value of our investments and have determined there was no impairment or observable price changes as of June 30, 2021.

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 of finished goods and related packaging components. We recorded inventory obsolescence expense of $29,834 for the six months ended June 30, 2021 and $75,422 for the six months ended June 30, 2020. The allowance for obsolete and slow-moving inventory had a balance of $295,841 at June 30, 2021, and $276,603 at June 30, 2020. We considered the impact of COVID-19 on its recorded value of inventory and determined no adjustment was necessary as of June 30, 2021.

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Use of Estimates

The preparation of financial position, operations or cash flows.


Contractual Commitments
Royalty agreement. Effective November 28, 2007, WCI entered into separate exclusive license agreementsstatements in conformity with Applied Nutritionals, LLC (“Applied”)generally accepted accounting principles requires management to make estimates and its founder George Petito, pursuantassumptions that affect amounts reported in the financial statements and accompanying notes. The extent to which WCI obtained the exclusive world-wide licenseCOVID-19 pandemic may directly or indirectly impact our business, financial condition, and results of operations is highly uncertain and subject to make products incorporating intellectual property covered bychange. We considered the potential impact of the COVID-19 pandemic on our estimates and assumptions and determined there was not a patent related to CellerateRX products. In considerationmaterial impact on our estimates and assumptions used in preparing our consolidated financial statements as of and for the licenses, WCI agreedsix months ended June 30, 2021; however, actual results could differ from those estimates and there may be changes to pay to Applied  the following royalties, beginning January 3, 2008: (a) an upfront royalty of $100,000our estimates in the aggregate, (b) an aggregate royalty of fifteen percent (15%) of gross sales occurring during the first year of the license; (c) an additional upfront royalty of $400,000, in the aggregate, which was paid October, 2009; plus (d) an aggregate royalty of three percent (3%) of gross sales for all sales occurring after the payment of the $400,000 upfront royalty. In addition, WCI must maintain a minimum aggregate annual royalty payment of $375,000 for 2009 and thereafter, if the royalty payments made do not meet or exceed that amount.  The total of unpaid royalties as of December 31, 2016 was $276,916. These prior year royalties were paid in full in March of 2016. As of September 30, 2017, the balance of accrued royalties for the current year is $232,511.
future periods.

Off-Balance Sheet Arrangements

None.

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

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 (“SEC”) under the Securities Exchange Act, of 1934, as amended, is recorded, processed, summarized and reported within the time periods specified by the Securities and Exchange Commission’sSEC’s rules and forms, and that information is accumulated and communicated to our management, including our principal executive and principal financial officerofficers (whom we refer to in this periodic report as our Certifying Officer)Officers), as appropriate to allow timely decisions regarding required disclosure. Our management evaluated, with the participation of our Certifying Officer,Officers, the effectiveness of our disclosure controls and procedures as of SeptemberJune 30, 2017,2021, pursuant to Rule 13a-15(b) under the Securities Exchange Act. Based upon that evaluation, our Certifying OfficerOfficers concluded that, as of SeptemberJune 30, 2017,2021, 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 our most recently completed fiscalthe quarter ended June 30, 2021 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.  We will continue to evaluate the effectiveness of internal controls and procedures on an on-going basis.

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Part II — Other Information

Item 1. Legal Proceedings

None.

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

As

Other than as described 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, 2020. For more information concerning our risk factors, please see “Item 1A. Risk Factors” in the Form 10-K for the year ended December 31, 2020.

Historically, we have relied heavily on third parties to file and pursue the applications necessary to gain regulatory approvals for the products we market and license. We now expect to have the capability to develop certain of our pipeline candidates in-house, and will be subject to FDA requirements as well as other regulations applicable to medical product manufacturers.

On July 14, 2021, we entered into an asset purchase agreement with Rochal Industries LLC (“Rochal”), effective July 1, 2021, pursuant to which we purchased certain assets of Rochal, including, among others, intellectual property, FDA 510(k) clearances for four medical devices, rights to license certain product candidates and technologies currently under development, equipment, and supplies. Through the asset purchase, our pipeline now contains products and product candidates intended for mitigation of opportunistic pathogens and biofilm, wound re-epithelialization and closure, necrotic tissue debridement, and cell compatible substrates. Historically, we have relied heavily on third parties to file and pursue the applications necessary to gain regulatory approvals for the products we market and license. We now expect to have the capability to develop certain of our pipeline candidates in-house, and will be subject to FDA requirements, including the FDA’s current good manufacturing practices (“cGMP”), current good tissue practices (“cGTP”), and the Quality System Regulation (“QSR”), as applicable, as well as other regulations applicable to medical product manufacturers. While we previously relied on our research and development partners to pursue regulatory approvals for the products we market and license, we will now be responsible for gaining approval of certain of our product candidates through regulatory bodies on our own. We may be unable to comply with applicable FDA, state and foreign regulatory requirements and may not be able to successfully commercialize our products on our own, which could have a smaller reporting company, we are not required to provide this information.

material adverse effect on our business.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

None.

There were no sales of unregistered securities during the quarter ended June 30, 2021 that were not previously reported on a Current Report on Form 8-K.

Item 3. Defaults Upon Senior Securities

None.

Item 4. Mine Safety Disclosure

This item is not applicable.

Item 5. Other Information

None.


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Item 6. Exhibits

The following documents are filed as part of this Report:

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).

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*

Modification Agreement to Loan Agreement, dated January 15, 2021, between the Company, as Borrower, and Cadence Bank, N.A, as Lender.

10.2

Consulting Agreement, dated July 14, 2021, by and between Sanara MedTech Inc. and Ann Beal Salamone (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K of the Company filed on July 19, 2021 by the Company with the SEC).

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*2002.

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*2002.

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*2002.

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*2002.

101.CAL

Inline XBRL Calculation Linkbase Document.

101.DEF

Inline XBRL Definition Linkbase Document.

101.LAB

Inline XBRL Label Linkbase Document.

101.PRE

Inline XBRL Presentation Linkbase Document.

104

Cover Page Interactive Data File (Formatted as Inline XBRL and contained in Exhibit 101).

* Filed herewith

# Schedules have been omitted pursuant to Item 601(b)(2) of Regulation S-K. Sanara MedTech Inc. hereby undertakes to furnish supplementally copies of any of the omitted schedules upon request by the Securities and Exchange Commission.

** 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 Annual Report on Form 10-K, irrespective of any general incorporation language contained in such filing.

 
10129

Interactive Data Files pursuant to Rule 405Table of Regulation S-T.Contents
*  Filed herewith

Signatures

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.

Wound Management Technologies, Inc.

SANARA MEDTECH INC.

August 16, 2021

By:

/s/ Michael McNeil

Michael McNeil

Chief Financial Officer

(Principal Financial Officer and duly authorized officer)

 
30
November 16, 2017By:/s/ J. Michael Carmena
J. Michael Carmena,
Chief Financial Officer
 17