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PAVmed (NASDAQ: PAVM) overhauls capital structure and reports 2025 results

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Rhea-AI Filing Summary

PAVmed Inc. reported fourth quarter and full year 2025 results and detailed major balance sheet and business changes. For the three months ended December 31, 2025, revenue was $52,000, operating expenses were about $6.9 million, and GAAP net loss attributable to common stockholders was approximately $1.8 million, or $(2.05) per diluted share. Non-GAAP adjusted loss was about $0.9 million, or $(1.05) per share.

The company raised $30 million through a Series D preferred stock offering and $15 million via senior secured notes, using part of the proceeds to eliminate all previously outstanding convertible securities and extend its cash runway. It also issued $30 million in Series D warrants linked to a draft CMS coverage policy for Lucid’s EsoGuard test, reported cash and cash equivalents of $1.5 million as of December 31, 2025, and highlighted progress at subsidiaries Lucid Diagnostics and Veris Health, including a VA contract for EsoGuard, large real-world data on esophageal precancer detection, and advancement of an implantable physiological monitor toward a planned late 2026 FDA 510(k) submission.

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Insights

PAVmed reshapes its capital structure while subsidiaries advance key programs.

PAVmed combined 2025 results with a substantial recapitalization. It completed a $30 million Series D preferred stock offering and a $15 million senior secured note financing, using part of the proceeds to eliminate all previously outstanding convertible securities and remove a legacy capital overhang.

Operating performance remains modest, with Q4 2025 revenue of $52,000 and a GAAP net loss attributable to common stockholders of about $1.8 million, alongside a non-GAAP adjusted loss of roughly $0.9 million. Cash and cash equivalents were $1.5 million as of December 31, 2025, only slightly higher than a year earlier.

Subsidiaries provide much of the strategic narrative. Lucid Diagnostics generated $1.5 million in Q4 2025 EsoGuard revenue, processed 3,664 tests, secured a U.S. Veterans Affairs contract, and reported positive real-world data in nearly 12,000 patients. Veris Health progressed a strategic engagement with OSU-The James and is working toward a planned late 2026 FDA 510(k) submission for its implantable physiological monitor.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 20549

 

FORM 8-K

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d) OF THE

SECURITIES EXCHANGE ACT OF 1934

 

Date of Report (Date of earliest event reported): March 30, 2026

 

PAVMED INC.
(Exact Name of Registrant as Specified in Charter)

 

Delaware   001-37685   47-1214177
(State or Other Jurisdiction
of Incorporation)
  (Commission
File Number)
  (IRS Employer
Identification No.)

 

360 Madison Avenue, 25th Floor, New York, New York   10017
(Address of Principal Executive Offices)   (Zip Code)

 

Registrant’s telephone number, including area code: (917) 813-1828

 

N/A
(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425).
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12).
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)).
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)).

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Common Stock, Par Value $0.001 Per Share   PAVM   The Nasdaq Stock Market LLC

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

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. ☐

 

 

 

 
 

 

Item 2.02. Results of Operations and Financial Condition.

 

On March 30, 2026, PAVmed Inc. (the “Company”) issued a press release announcing financial results for its fiscal year ended December 31, 2025 and providing a business update. A copy of the press release is attached to this report as Exhibit 99.1 and is incorporated herein by reference.

 

Item 7.01. Regulation FD Disclosure.

 

The disclosure set forth under Item 2.02 is incorporated herein by reference.

 

The information furnished under Items 2.02 and 7.01, including the exhibit related thereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall it be deemed incorporated by reference in any disclosure document of the Company, except as shall be expressly set forth by specific reference in such document.

 

Item 9.01. Financial Statements and Exhibits.

 

(d) Exhibits:

 

Exhibit No.   Description
99.1   Press release.
104   Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

 
 

 

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

Dated: March 30, 2026 PAVMED INC.
   
  By: /s/ Dennis McGrath
    Dennis McGrath
    President and Chief Financial Officer

 

 

 

 

Exhibit 99.1

 

PAVmed Provides Business Update and Reports Fourth Quarter and Full Year 2025 Financial Results

 

PAVmed strengthened its capital structure and relaunched its medical device portfolio under new leadership

 

Veris Health advanced strategic partnership with OSU and progressed implantable physiological monitor toward FDA submission

 

Lucid Diagnostics expanded EsoGuard healthcare system access and clinical evidence base

 

Conference call and webcast to be held today, March 30, at 8:30 AM EST

 

NEW YORK, March 30, 2026 - PAVmed Inc. (NASDAQ: PAVM) (“PAVmed” or the “Company”), a diversified commercial-stage medical technology company, operating in the medical device, diagnostics, and digital health sectors, today provided a business update for the Company and its subsidiaries, Lucid Diagnostics Inc. (NASDAQ: LUCD) (“Lucid”) and Veris Health Inc. (“Veris”), and reported financial results for the fourth quarter and year ended December 31, 2025.

 

Conference Call and Webcast

 

The webcast will take place on Monday, March 30, 2026, at 8:30 AM and is accessible in the investor relations section of the Company’s website at pavmed.com. Alternatively, to access the conference call by telephone, U.S.-based callers should dial 1-800-836-8184 and international listeners should dial 1-646-357-8785. All listeners should provide the operator with the conference call name “PAVmed Business Update” to join.

 

Following the conclusion of the conference call, a replay will be available for 30 days on the investor relations section of the Company’s website at pavmed.com.

 

Business Update Highlights

 

“Over the past two years, we’ve undertaken a series of deliberate, systematic actions to fix PAVmed’s legacy capital structure and strengthen its balance sheet,” said Lishan Aklog, M.D., PAVmed’s Chairman and Chief Executive Officer. “This process is now complete and we believe PAVmed is exceptionally well positioned to execute on its founding mission — to operate as a high-growth diversified commercial life sciences company with multiple independently financed subsidiaries operating under a shared services model. Veris is now well underway in the commercial phase of its strategic engagement with OSU-The James while progressing its implantable physiological monitor toward FDA submission. Lucid continues to maintain a strong commercial foundation as it approaches transformative Medicare coverage for EsoGuard. We have also relaunched PAVmed’s medical device portfolio under experienced leadership and completed the licensing of our endoscopic esophageal imaging technology from Duke University, adding another potential growth engine to our pipeline.”

 

 
 

 

Highlights from the fourth quarter and recent weeks:

 

PAVmed strengthened its balance sheet through the completion of a $30 million Series D preferred stock offering and a $15 million senior secured note financing. A portion of the proceeds from these activities was used to eliminate all previously outstanding convertible securities, removing a significant legacy capital structure overhang and extending the Company’s cash runway. In addition, the Company issued $30 million in Series D warrants, which are callable upon the publication of a draft CMS coverage policy for Lucid’s EsoGuard Esophageal DNA Test.

 

PAVmed relaunched its medical device portfolio and appointed industry veteran Joseph Virgilio as Chief Business Officer of Medical Devices to oversee development and commercialization of its current and future device portfolio, including the PortIO implantable intraosseous vascular access device and endoscopic esophageal imaging technology licensed from Duke University.

 

Veris advanced its strategic engagement with The Ohio State University’s James Cancer Hospital, with the commercial phase well underway and full integration with the hospital’s electronic health record (EHR) system now complete.

Veris is engaged with its development and manufacturing partner for its implantable physiological monitor, supporting a planned late 2026 FDA 510(k) submission.

 

Lucid Diagnostics announced fourth quarter and full year 2025 financial results and key business developments, including:

 

Recognized $1.5 million in EsoGuard® Esophageal DNA Test revenue for 4Q25 and processed 3,664 EsoGuard tests.

 

Awarded U.S. Department of Veterans Affairs (VA) contract for EsoGuard, expanding access across the nation’s largest integrated healthcare system serving approximately nine million veterans.

 

Announced positive data from the largest reported real-world experience of esophageal precancer detection, evaluating Lucid’s EsoGuard and EsoCheck® Esophageal Cell Collection Device in nearly 12,000 at-risk patients.

 

Financial Results:

 

For the three months ended December 31, 2025, Operating expenses were approximately $6.9 million which include stock-based compensation expenses of $0.3 million. GAAP net loss attributable to common stockholders was approximately $1.8 million, or $(2.05) per common share on a diluted basis.

 

As shown below and for the purpose of illustrating the effect of stock-based compensation and other non-cash income and expenses on the Company’s financial results, the Company’s non-GAAP adjusted loss was approximately $0.9 million or $(1.05) per common share.

 

 
 

 

PAVmed had cash and cash equivalents of $1.5 million as of December 31, 2025, compared to $1.2 million as of December 31, 2024.

 

The audited financial results for the year ended December 31, 2025 were filed with the SEC on Form 10-K on March 27, 2026, and are available at www.pavmed.com or www.sec.gov.

 

PAVmed Non-GAAP Measures

 

To supplement our financial results presented in accordance with U.S. generally accepted accounting principles (GAAP), management provides certain non-GAAP financial measures of the Company’s financial results. These non-GAAP financial measures include net loss before interest, taxes, depreciation, and amortization (EBITDA) and non-GAAP adjusted loss, which further adjusts EBITDA for stock-based compensation expense, loss on the issuance or modification of convertible securities, the periodic change in fair value of convertible securities, and loss on debt extinguishment. The foregoing non-GAAP financial measures of EBITDA and non-GAAP adjusted loss are not recognized terms under U.S. GAAP.

 

Non-GAAP financial measures are presented with the intent of providing greater transparency to the information used by us in our financial performance analysis and operational decision-making. We believe these non-GAAP financial measures provide meaningful information to assist investors, shareholders, and other readers of our financial statements in making comparisons to our historical financial results and analyzing the underlying performance of our results of operations. These non-GAAP financial measures are not intended to be, and should not be, a substitute for, considered superior to, considered separately from, or as an alternative to, the most directly comparable GAAP financial measures.

 

Non-GAAP financial measures are provided to enhance readers’ overall understanding of our current financial results and to provide further information for comparative purposes. Management believes the non-GAAP financial measures provide useful information to management and investors by isolating certain expenses, gains, and losses that may not be indicative of our core operating results and business outlook. Specifically, the non-GAAP financial measures include non-GAAP adjusted loss, and its presentation is intended to help the reader understand the effect of the loss on the issuance or modification of convertible securities, the periodic change in fair value of convertible securities, the loss on debt extinguishment and the corresponding accounting for non-cash charges on financial performance. In addition, management believes non-GAAP financial measures enhance the comparability of results against prior periods.

 

 
 

 

A reconciliation to the most directly comparable GAAP measure of all non-GAAP financial measures included in this press release for the three months and year ended December 31, 2025 and 2024 are as follows:

 

Condensed Consolidated Statement of Operations (Unaudited)

 

   For the three months ended
December 31,
   For the year ended
December 31,
 
   2025   2024   2025   2024 
(in thousands except per-share amounts)                
Revenue  $52   $10   $71   $2,995 
Operating expenses   6,853     5 198     21,877    47,482 
Other (Income) Expense   (4,046)   (6 330)    (19,337)   (72,914)
Net (Income) Loss   2,755    (1,142)   2,469    (28,427)
Net income (loss) per common share, diluted  $(2.05)  $3.60   $(5.63)  $14.90 
Net income (loss) attributable to common stockholders   (1,832)   1,346    (3,774)   31,966 
Preferred Stock dividends and deemed dividends   569    85    4,175    7,825 
Net income (loss) as reported   (1,263)   1,431    401    39,791 
Adjustments:                    
Depreciation and amortization expense1   18    69    105    1,198 
Interest expense, net2       4    (8)   (209)
NCI ownership share of Interest and Depreciation adjustments   (715)       (715)   (229)
EBITDA   (1,960)   1,504    (217)   40,551 
                     
Other non-cash or financing related expenses:                    
Stock-based compensation expense3   232    733    1,707    6,449 
Operating expenses issued in stock1   350    150    505    598 
Gain on deconsolidation of subsidiary               (72,287)
Change in FV equity method investments   (2,504)   (125)   (8,483)   (532)
Change in FV convertible debt2   2,940    (2,950)   3,249    (462)
Loss on debt extinguishment2           58    2,535 
Debt modification expense               2,000 
NCI ownership share of non-GAAP adjustments               (1,262)
Non-GAAP adjusted (loss)  $(942)  $(688)  $(3,141)  $(22,410)
Non-GAAP shares outstanding, basic and diluted   893    361    670    322 
Non-GAAP adjusted (loss) income per share, basic and diluted  $(1.05)  $(1.91)  $(4.69)  $(69.51)

 

1 Included in general and administrative expenses in the financial statements.

2 Included in other income and expenses.

3 Stock-based compensation (“SBC”) expense is included in operating expenses and is detailed as follows in the table below by category within operating expenses for the non-GAAP Net operating expenses:

 

 
 

 

Reconciliation of GAAP Operating Expenses to Non-GAAP Net Operating Expenses

 

(in thousands except per-share amounts)  For the three months ended
December 31,
   For the year ended
December 31,
 
   2025   2024   2025   2024 
                 
Cost of revenue  $86   $48   $218   $4,840 
Stock-based compensation expense3               (112)
Net cost of revenue   86    48    218    4,728 
                     
Amortization of acquired intangible assets               559 
                     
Sales and marketing   249    155    917    11,627 
Stock-based compensation expense3   (2)   (18)   (61)   (1,100)
Net sales and marketing   247    137    856    10,527 
                     
General and administrative   4,691    4,188    16,250    24,524 
Depreciation expense   (18)   (69)   (105)   (639)
Operating expenses issued in stock   (350)   (150)   (505)   (598)
Stock-based compensation expense3   (207)   (653)   (1,483)   (4,370)
Net general and administrative   4,116    3,316    14,157    18,917 
                     
Research and development   1,827    807    4,492    5,932 
Stock-based compensation expense3   (23)   (62)   (163)   (867)
Net research and development   1,804    745    4,329    5,065 
                     
Total operating expenses   6,853    5,198    21,877    47,482 
Depreciation and amortization expense   (18)   (69)   (105)   (1,198)
Operating expenses issued in stock   (350)   (150)   (505)   (598)
Stock-based compensation expense3   (232)   (733)   (1,707)   (6,449)
Net operating expenses  $6,253   $4,246   $19,560   $39,237 

 

 
 

 

About PAVmed and its Subsidiaries

 

PAVmed Inc. is a diversified commercial-stage medical technology company operating in the medical device, diagnostics, and digital health sectors. Its subsidiary, Lucid Diagnostics Inc. (NASDAQ: LUCD), is a commercial-stage cancer prevention medical diagnostics company that markets the EsoGuard® Esophageal DNA Test and EsoCheck® Esophageal Cell Collection Device—the first and only commercial tools for widespread early detection of esophageal precancer to mitigate the risks of esophageal cancer deaths. Its other subsidiary, Veris Health Inc., is a digital health company focused on enhanced personalized cancer care through remote patient monitoring using implantable biologic sensors with wireless communication along with a custom suite of connected external devices. Veris is concurrently developing an implantable physiological monitor, designed to be implanted alongside a chemotherapy port, which will interface with the Veris Cancer Care Platform.

 

For more and for more information about PAVmed, please visit pavmed.com.

 

For more information about Lucid Diagnostics, please visit luciddx.com.

 

For more information about Veris Health, please visit verishealth.com.

 

Forward-Looking Statements

 

This press release includes forward-looking statements that involve risks and uncertainties. Forward-looking statements are any statements that are not historical facts. Such forward-looking statements, which are based upon the current beliefs and expectations of PAVmed’s and Lucid’s management, are subject to risks and uncertainties, which could cause actual results to differ from the forward-looking statements. Risks and uncertainties that may cause such differences include, among other things, volatility in the price of PAVmed’s and Lucid’s common stock; general economic and market conditions; the uncertainties inherent in research and development, including the cost and time required to advance PAVmed’s and Lucid’s products to regulatory submission; whether regulatory authorities will be satisfied with the design of and results from PAVmed’s and Lucid’s clinical and preclinical studies; whether and when PAVmed’s and Lucid’s products are cleared by regulatory authorities; market acceptance of PAVmed’s and Lucid’s products once cleared and commercialized; PAVmed’s and Lucid’s ability to raise additional funding as needed; and other competitive developments. In addition, new risks and uncertainties may arise from time to time and are difficult to predict. For a further list and description of these and other important risks and uncertainties that may affect PAVmed’s and Lucid’s future operations, see Part I, Item 1A, “Risk Factors,” in PAVmed’s and Lucid’s most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission, as the same may be updated in Part II, Item 1A, “Risk Factors” in any Quarterly Report on Form 10-Q filed by PAVmed or Lucid after its most recent Annual Report. PAVmed and Lucid disclaim any intention or obligation to publicly update or revise any forward-looking statement to reflect any change in its expectations or in events, conditions, or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements.

 

Investor and Media Contact

 

Matt Riley

PAVmed and Lucid Diagnostics

mjr@pavmed.com

 

 

 

FAQ

How did PAVmed (PAVM) perform financially in Q4 2025?

PAVmed reported Q4 2025 revenue of $52,000, operating expenses of about $6.9 million, and a GAAP net loss attributable to common stockholders of roughly $1.8 million, or $(2.05) per diluted share, with non-GAAP adjusted loss near $0.9 million.

What capital structure changes did PAVmed (PAVM) make in 2025?

PAVmed completed a $30 million Series D preferred stock offering and a $15 million senior secured note financing. Part of the proceeds eliminated all previously outstanding convertible securities, reducing legacy capital structure overhang and extending the company’s cash runway, according to management’s comments.

What were PAVmed’s (PAVM) cash levels at year-end 2025?

PAVmed reported $1.5 million in cash and cash equivalents as of December 31, 2025, compared with $1.2 million as of December 31, 2024. This modest increase followed the Series D preferred and senior secured note financings described in the update.

How is Lucid Diagnostics, PAVmed’s subsidiary, performing with EsoGuard?

Lucid Diagnostics recognized $1.5 million in Q4 2025 EsoGuard Esophageal DNA Test revenue and processed 3,664 tests. It also secured a U.S. Department of Veterans Affairs contract for EsoGuard and reported positive data from nearly 12,000 at-risk patients in real-world esophageal precancer detection.

What progress did Veris Health, a PAVmed subsidiary, report?

Veris Health advanced its strategic engagement with The Ohio State University’s James Cancer Hospital, with the commercial phase underway and full EHR integration complete. It is also working with a development and manufacturing partner toward a planned late 2026 FDA 510(k) submission for an implantable physiological monitor.

What non-GAAP metrics did PAVmed (PAVM) highlight for 2025?

PAVmed emphasized non-GAAP adjusted loss, which for Q4 2025 was about $0.9 million, or $(1.05) per share. Management also referenced EBITDA and adjustments for stock-based compensation, convertible securities fair value changes, and debt-related items to isolate core operating performance.

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