Author: Ken Dropiewski

AngioDynamics to Report Fiscal 2026 Third Quarter Results on April 2, 2026

LATHAM, N.Y.–(BUSINESS WIRE)–AngioDynamics, Inc. (NASDAQ: ANGO), a leading and transformative medical technology company focused on restoring healthy blood flow in the body’s vascular system, expanding cancer treatment options and improving patient quality of life, today announced that it will report financial results for the third quarter of fiscal year 2026 before the market open on Thursday, April 2, 2026. The Company’s management will host a conference call at 8:00 am ET the same day to d

Heartflow Reports Fourth Quarter and Full Year 2025 Financial Results

MOUNTAIN VIEW, Calif., March 18, 2026 (GLOBE NEWSWIRE) — Heartflow, Inc. (Heartflow) (Nasdaq: HTFL), the leader in AI technology for coronary artery disease (CAD), today reported financial results for the fourth quarter and full year ended December 31, 2025. Fourth Quarter 2025 Highlights Total revenue of $49.1 million, a 40% increase year-over-yearGross margin of 79.5%, non-GAAP gross margin of 79.9%Net operating loss of $17.8 million, non-GAAP net operating loss of $12.5 millionU.S. installed base of 1,465 accounts as of December 31, 2025U.S. Plaque installed base of 489 accounts as of December 31, 2025Aetna began coverage of Heartflow Plaque Analysis, bringing total U.S. covered lives for Plaque to approximately 75% 2026 Annual Guidance Total revenue of $218 million to $222 million (approximately 24% to 26% growth year-over-year)Non-GAAP gross margin of 80% to 81% “Our strong fourth quarter performance concluded a record year for Heartflow,” said John Farquhar, President and CEO of Heartflow. “The accelerating adoption of the Heartflow Platform, combined with our disciplined execution across commercial, innovation, and clinical initiatives, drove 40% fourth quarter and full year revenue growth and record gross margins. We also made significant strides in scaling account activations and driving early physician adoption of Heartflow Plaque Analysis. Our 2026 guidance reflects strong business fundamentals, a solid foundation for growth, and high confidence in consistent execution. With commercial, innovation and clinical catalysts on the horizon, our conviction in the business has never been higher.” Fourth Quarter 2025 Financial ResultsTotal revenue was $49.1 million, a 40% increase year-over-year. U.S. revenue was $44.8 million, a 41% increase year-over-year. International and other revenue was $4.3 million, a 35% increase year-over-year. The year-over-year increase in total global revenue was primarily attributable to an increase in total U.S. FFRCT volume. Gross profit was $39.1 million, compared to $26.3 million in the prior year period. Non-GAAP gross profit was $39.2 million, compared to $26.3 million in the prior year period. Gross margin was 79.5%, compared to 75.0% in the prior year period. Non-GAAP gross margin was 79.9%, compared to 75.3% in the prior year period. The year-over-year gross margin expansion was primarily attributable to an increase in revenue case volume and improved production team productivity driven by AI efficiency initiatives, partially offset by the hiring and training of production team personnel. Total operating expenses were $56.8 million, or 116% of total revenue, compared to $42.3 million, or 121% of total revenue, in the prior year period. Non-GAAP total operating expenses were $51.7 million, or 105% of total revenue, compared to $39.9 million, or 114% of total revenue, in the prior year period. The year-over-year operating expense increase was primarily attributable to increased investment in sales personnel and related expenses, as well as increased investments in technology and clinical research. Net operating loss was $17.8 million, compared to $16.1 million in the prior year period. Non-GAAP net operating loss was $12.5 million, compared to $13.5 million in the prior year period. Net loss was $24.4 million, or ($0.29) net loss per share, compared to $33.0 million, or ($5.59) net loss per share, in the prior year period. Net loss for the fourth quarters of 2025 and 2024 included a noncash charge of $9.3 million and $11.9 million, respectively, resulting from the remeasurement of the fair value of the Company’s common stock warrant liability. As of October 22, 2025, the warrant holder net exercised all warrants in full. Therefore, the fourth quarter of 2025 is the last quarter that movements in the Company’s stock price will trigger a warrant revaluation and result in a noncash charge to net loss. Non-GAAP net loss was $9.8 million, or ($0.12) non-GAAP net loss per share, compared to $18.6 million, or ($3.15) non-GAAP net loss per share, in the prior year period. Adjusted EBITDA was ($11.1) million, compared to ($12.0) million in the prior year period. Full Year 2025 Financial ResultsTotal revenue was $176.0 million, a 40% increase year-over-year. U.S. revenue was $160.6 million, a 41% increase year-over-year. International and other revenue was $15.4 million, a 26% increase year-over-year. The year-over-year increase in total global revenue was primarily attributable to an increase in total U.S. FFRCT volume. Gross profit was $135.2 million, compared to $94.4 million in the prior year period. Non-GAAP gross profit was $135.6 million, compared to $94.8 million in the prior year period. Gross margin was 76.8%, compared to 75.1% in the prior year period. Non-GAAP gross margin was 77.0%, compared to 75.3% in the prior year period. The year-over-year gross margin expansion was primarily attributable to an increase in revenue case volume and improved production team productivity driven by AI efficiency initiatives, partially offset by the hiring and training of production team personnel. Total operating expenses were $199.3 million, or 113% of total revenue, compared to $155.7 million, or 124% of total revenue, in the prior year period. Non-GAAP total operating expenses were $185.7 million, or 105% of total revenue, compared to $145.8 million, or 116% of total revenue, in the prior year period. The year-over-year operating expense increase was primarily attributable to increased investment in personnel and related expenses, as well as increased investments in technology and clinical research. Net operating loss was $64.1 million, compared to $61.2 million in the prior year period. Non-GAAP net operating loss was $50.1 million, compared to $51.0 million in the prior year period. Net loss was $116.8 million, or ($3.17) net loss per share, compared to $96.4 million, or ($17.98) net loss per share, in the prior year period. Non-GAAP net loss was $59.9 million, or ($1.62) non-GAAP net loss per share, compared to $69.6 million, or ($12.98) non-GAAP net loss per share, in the prior year period. Adjusted EBITDA was ($44.7) million, compared to ($45.7) million in the prior year period. Cash, cash equivalents and investments totaled $280.2 million as of December 31, 2025. For additional information regarding non-GAAP financial measures, see “Use of Non-GAAP Measures,” “Heartflow GAAP to Non-GAAP Reconciliations” and “Reconciliation of GAAP Net Loss to Adjusted EBITDA” below. Webcast and Conference Call DetailsHeartflow will host a conference call today, March 18, 2026, at 1:30 p.m. PT / 4:30 p.m. ET to discuss its fourth quarter and full year 2025 financial results. Those interested in listening to the conference call should register online using this link. Once registered, participants will receive dial-in numbers and a unique PIN to join the call. Participants are encouraged to register more than 15 minutes prior to the start of the call. A live and archived webcast of the event will also be available on the “Investor Relations” section of the Heartflow website at https://ir.heartflow.com. The archived version will be available for 12 months following completion of the live call. About Heartflow’s Technology and ResearchHeartflow’s technology is redefining precision cardiovascular care through clinically-proven AI and the world’s largest coronary imaging dataset. Heartflow has been adopted by more than 1,800 institutions globally and continues to strengthen its commercial presence to make this cutting-edge solution more widely available to an increasingly diverse patient population. Backed by American College of Cardiology and American Heart Association (ACC/AHA) guidelines and supported by more than 600 peer-reviewed publications, Heartflow has redefined how clinicians manage care for over 600,000 patients worldwide.1 Key benefits include: Proprietary data pipeline: Built from more than 160 million annotated CTA images, Heartflow’s data foundation powers advanced AI models that deliver highly accurate, reproducible insights across diverse patient populations.Extensive clinical and real-world validation: Heartflow’s AI-driven solutions have been validated through clinical evidence in over 200 studies assessing over 365,000 patients. Proven in real-world practice with reproducibility and accuracy, Heartflow’s coronary CTA image acceptance rates exceed 97%.Seamless clinical integration via upgraded workflow: Heartflow delivers final quality-reviewed analyses instantly upon order, enabling clinicians to move from diagnosis to decision without delay.Quality system, global security and patient-data integrity compliance: Heartflow meets or exceeds leading international standards, including HITRUST, SOC 2 Type 2, ISO 13485, and ISO 27001. About Heartflow, Inc.Heartflow is transforming coronary artery disease from the world’s leading cause of death into a condition that can be detected early, diagnosed accurately, and managed for life. The Heartflow One platform uses AI to turn coronary CTA images into personalized 3D models of the heart, providing clinically meaningful, actionable insights into plaque location, volume, and composition and its effect on blood flow — all without invasive procedures. Discover how we’re shaping the future of cardiovascular care at heartflow.com. Use of Non-GAAP MeasuresTo supplement its consolidated financial statements prepared in accordance with U.S. generally accepted accounting principles (GAAP), the Company discloses non-GAAP gross profit and non-GAAP gross margin, non-GAAP total operating expenses, non-GAAP research and development expense, non-GAAP selling, general and administrative expense, non-GAAP net operating loss, non-GAAP net loss, non-GAAP net loss per share, basic and diluted, and Adjusted EBITDA (collectively, the “Non-GAAP Measures”) in this press release. As used by the Company, these measures are adjusted to exclude stock-based compensation expense from the comparable GAAP financial measure. Non-GAAP net loss and non-GAAP net loss per share, basic and diluted, are also adjusted for change in fair value of common stock warrant liability, change in fair value of derivative liability and loss on extinguishment of debt. In addition, Adjusted EBITDA is calculated by adding back to net loss or excluding, as appropriate, interest income and expense, provision for income taxes, and charges for depreciation and amortization and is further adjusted by adding back in or excluding, stock-based compensation and, as appropriate, other income and expense items that are not reflective of the Company’s underlying continuing operating performance. Reconciliations of the Non-GAAP Measures to their most directly comparable GAAP financial measures are provided in the financial statement tables included at the end of this press release, and investors are encouraged to review the reconciliations. The Company believes the presentation of the Non-GAAP Measures, when shown in conjunction with the corresponding GAAP measures, provides useful information to investors as it provides visibility to the Company’s underlying continuing operating performance from period to period by excluding the impact of stock-based compensation and certain other items that are not reflective of the Company’s ongoing operations. Because of the variety of equity awards used by companies, the varying methodologies for determining stock-based compensation expense, the subjective assumptions used in those determinations, and the volatility in valuations that can be driven by market conditions outside the Company’s control, we believe excluding stock-based compensation expense enhances the ability of management and investors to understand and assess the underlying performance of our business over time and compare it against our peers, a majority of whom also exclude stock-based compensation expense from their non-GAAP results. With respect to the presentation of Adjusted EBITDA, the Company believes it is a useful measure to evaluate the Company’s operating performance and it is used by the Company to evaluate ongoing operations and for planning and forecasting purposes. Adjusted EBITDA is also a measure frequently used by analysts, investors and other interested parties to evaluate companies in our same industry. The Company’s definition of the Non-GAAP Measures may differ from similarly titled measures used by others. The Non-GAAP Measures should be considered only as a supplement to, and not as a substitute for, or superior to, their most directly comparable GAAP financial measures. Because the Non-GAAP Measures exclude the effect of items that increase or decrease the Company’s reported results of operations, management strongly encourages investors to review the reconciliations to the most comparable GAAP financial measures at the end of this press release and, when they become available, the Company’s consolidated financial statements and publicly filed Securities and Exchange Commission (“SEC”) reports in their entirety. The Company is not able to provide a reconciliation without unreasonable efforts of its forward-looking guidance related to non-GAAP gross margin to the most directly comparable GAAP financial measure due to the unknown effect of stock-based compensation that is material to the comparable GAAP financial measure. Forward-Looking StatementsThis press release contains express or implied forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements other than statements of historical facts contained in this press release, including statements regarding our strategy, expected market growth and financial guidance, are forward-looking statements. These forward-looking statements are based on management’s current expectations and are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements, including, but not limited to: we may not be able to achieve or sustain profitability; our dependence on the success of our one product, Heartflow FFRCT Analysis; healthcare providers may be unwilling to change their standard practice regarding the evaluation of coronary artery disease; adoption of the Heartflow Platform by healthcare providers may be negatively impacted if third-party payors, including government payors, do not cover or provide adequate reimbursement; the concentration of our customer base; the significant competition we face in an environment of rapid technological change; the commercialization of Heartflow Plaque Analysis is nascent; risks associated with our use and development of AI models; risks related to failing to properly manage our future growth; disruption by catastrophic events; risks associated with our dependence on our information technology systems; security breaches that we cannot anticipate or successfully defend; extensive regulatory requirements we face to bring our products to market; and third parties could develop and commercial technology and products similar or identical to ours. For a more extensive description of these and other risks and uncertainties that could materially affect our results, you should read our filings with the SEC, including our Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, as such filings may be amended, supplemented or superseded from time to time by other reports Heartflow files with the SEC. You should not place undue reliance on the forward-looking statements in this press release, which speak only as of the date hereof, and we undertake no obligation to update the forward-looking statements to reflect events or circumstances after the date of this press release or to reflect new information or the occurrence of unanticipated events, except as required by law. Investor ContactNick Laudiconlaudico@heartflow.com Media ContactElliot Levyelevy@heartflow.com Heartflow, Inc.Consolidated Statements of Operations(unaudited, in thousands, except share and per share data)                            Three Months Ended Year Ended  December 31, December 31,   2025   2024   2025   2024              Revenue $49,130  $34,977  $176,034  $125,808 Cost of revenue  10,067   8,727   40,837   31,359 Gross profit  39,063   26,250   135,197   94,449 Operating Expenses:            Research and development  18,665   12,279   64,918   43,517 Selling, general and administrative  38,148   30,029   134,345   112,154 Total operating expenses  56,813   42,308   199,263   155,671 Loss from operations  (17,750)  (16,058)  (64,066)  (61,222)Interest income  2,635   592   5,538   4,066 Interest expense  (8)  (5,152)  (15,173)  (22,768)Change in fair value of common stock warrant liability  (9,308)  (11,905)  (43,894)  (16,395)Change in fair value of derivative liability  –   –   7,311   (222)Loss on extinguishment of debt  –   –   (6,360)  – Other income (expense), net  (129)  (447)  (223)  168 Loss before provision for income taxes  (24,560)  (32,970)  (116,867)  (96,373)(Provision for) benefit from income taxes  165   (5)  76   (53)Net loss $(24,395) $(32,975) $(116,791) $(96,426)Comprehensive loss:            Net loss $(24,395) $(32,975) $(116,791) $(96,426)Other comprehensive income (loss):            Foreign currency translation gain (loss)  (69)  233   191   (271)Unrealized gain on investments, net  156   –   156   – Total other comprehensive income (loss)  87   233   347   (271)Total comprehensive loss $(24,308) $(32,742) $(116,444) $(96,697)             Net loss per share, basic and diluted $(0.29) $(5.59) $(3.17) $(17.98)Weighted-average shares used to compute net loss per share, basic and diluted 84,828,694   5,894,840   36,853,867   5,363,435  Heartflow, Inc.Consolidated Balance Sheets(unaudited, in thousands)         December 31,  2025 2024Assets      Current assets      Cash and cash equivalents $44,776  $51,367 Short-term investments  132,010   – Accounts receivable, net  29,343   24,639 Restricted cash, current  –   150 Prepaid expenses and other current assets  14,075   6,132 Total current assets  220,204   82,288 Long-term investments  103,365   – Property and equipment, net  8,587   8,920 Operating lease right-of-use assets  17,488   18,805 Restricted cash, non-current  4,709   4,325 Other non-current assets  5,099   4,366 Total assets $359,452  $118,704        Liabilities, redeemable convertible preferred stock and stockholders’ equity (deficit)      Current liabilities      Accounts payable $3,169  $2,870 Accrued expenses and other current liabilities  33,279   25,319 Operating lease liabilities, current portion  5,922   5,416 Total current liabilities  42,370   33,605 Term loan  –   136,431 Common stock warrant liability  –   20,835 Operating lease liabilities, non-current portion  16,132   18,537 Other non-current liabilities  303   214 Total liabilities  58,805   209,622 Redeemable convertible preferred stock issuable in series, $0.001 par value  –   768,566 Stockholders’ equity (deficit)      Preferred stock, $0.001 par value  –   – Common stock, $0.001 par value  85   6 Additional paid-in capital  1,388,737   112,241 Accumulated other comprehensive income  (425)  (772)Accumulated deficit  (1,087,750)  (970,959)Total stockholders’ equity (deficit)  300,647   (859,484)   Total liabilities, redeemable convertible preferred stock and stockholders’ equity (deficit)$359,452  $118,704  Heartflow, Inc.GAAP to Non-GAAP Reconciliations(unaudited, in thousands except per share amounts and percentage data)                Three Months Ended December 31, 2025  Three Months Ended December 31, 2024   GAAP  Adjustments  Non-GAAP  GAAP  Adjustments  Non-GAAP                   Gross profit $39,063  $184 (a)$39,247  $26,250  $76 (a)$26,326 Gross margin  79.5%  0.4%  79.9%  75.0%  0.2%  75.3%                   Operating Expenses:                  Research and development $18,665  $(1,547)(a)$17,118  $12,279  $(585)(a)$11,694 Selling, general and administrative $38,148  $(3,529)(a)$34,619  $30,029  $(1,853)(a)$28,176 Total operating expenses $56,813  $(5,076) $51,737  $42,308  $(2,438) $39,870                    Loss from operations $(17,750) $5,260  $(12,490) $(16,058) $2,514  $(13,544)                   Net loss $(24,395) $14,568 (b)$(9,827) $(32,975) $14,419 (c)$(18,556)Net loss per share, basic and diluted $(0.29) $0.17  $(0.12) $(5.59) $2.44  $(3.15)                   (a) Represents adjustments related to stock-based compensation expense(b) Represents adjustments for: (i) stock-based compensation expense of $5.3 million; and (ii) change in fair value of common stock warrant liability of $9.3 million(c) Represents adjustments for: (i) stock-based compensation expense of $2.5 million; and (ii) change in fair value of common stock warrant liability of $11.9 million    Heartflow, Inc.GAAP to Non-GAAP Reconciliations(unaudited, in thousands except per share amounts and percentage data)                Year Ended December 31, 2025  Year Ended December 31, 2024   GAAP  Adjustments  Non-GAAP  GAAP  Adjustments  Non-GAAP                   Gross profit $135,197  $413 (a)$135,610  $94,449  $307 (a)$94,756 Gross margin  76.8%  0.2%  77.0%  75.1%  0.2%  75.3%                   Operating Expenses:                  Research and development $64,918  $(3,434)(a)$61,484  $43,517  $(2,151)(a)$41,366 Selling, general and administrative $134,345  $(10,118)(a)$124,227  $112,154  $(7,755)(a)$104,399 Total operating expenses $199,263  $(13,552) $185,711  $155,671  $(9,906) $145,765                    Loss from operations $(64,066) $13,965  $(50,101) $(61,222) $10,213  $(51,009)                   Net loss $(116,791) $56,908 (b)$(59,883) $(96,426) $26,830 (c)$(69,596)Net loss per share, basic and diluted $(3.17) $1.55  $(1.62) $(17.98) $5.00  $(12.98)                   (a) Represents adjustments related to stock-based compensation expense(b) Represents adjustments for: (i) stock-based compensation expense of $14.0 million; (ii) change in fair value of common stock warrant liability of $43.9 million; (iii) change in fair value of derivative liability of $7.3 million; and (iv) loss on extinguishment of debt of $6.4 million(c) Represents adjustments for: (i) stock-based compensation expense of $10.2 million; (ii) change in fair value of common stock warrant liability of $16.4 million; and (iii) change in fair value of derivative liability of $0.2 million Heartflow, Inc.Reconciliation of GAAP Net Loss to Adjusted EBITDA(unaudited, in thousands)               Three Months Ended  Year Ended  December 31,  December 31,  2025 2024 2025 2024             GAAP net loss $(24,395) $(32,975) $(116,791) $(96,426)Non-GAAP adjustments:            Interest (income) expense, net  (2,627)  4,560   9,635   18,702 Change in fair value of common stock warrant liability  9,308   11,905   43,894   16,395 Change in fair value of derivative liability  –   –   (7,311)  222 Loss on extinguishment of debt  –   –   6,360   – Other (income) expense, net  129   447   223   (168)Provision for (benefit from) income taxes  (165)  5   (76)  53 Depreciation and amortization  1,371   1,591   5,440   5,358 Stock-based compensation expense  5,260   2,514   13,965   10,213 Adjusted EBITDA $(11,119) $(11,953) $(44,661) $(45,651) 1 Gulati, et al. 2021 AHA/ACC/ASE/CHEST/SAEM/SCCT/SCMR Guideline for the Evaluation & Diagnosis of Chest Pain. J Am Coll Cardiol.

JenaValve Announces FDA Approval of the Trilogy™ Transcatheter Heart Valve System — the First and Only Transcatheter Device Approved for Symptomatic, Severe Aortic Regurgitation (ssAR) in the United States

Approval marks a historic milestone for Americans living with ssAR who are at high risk for surgery and previously had no dedicated transcatheter treatment option Approval marks a historic milestone for Americans living with ssAR who are at high risk for surgery and previously had no dedicated transcatheter treatment option

Kestra Medical Technologies Reports Third Quarter Fiscal 2026 Financial Results

KIRKLAND, Wash., March 17, 2026 (GLOBE NEWSWIRE) — Kestra Medical Technologies, Ltd. (Nasdaq: KMTS), a leading wearable medical device and digital healthcare company, today reported financial results for the third quarter fiscal 2026, which ended January 31, 2026. Financial Highlights Generated revenue of $24.6 million in Q3 FY26, an increase of 63% compared to the prior year period.Expanded gross margin to 52.6% in Q3 FY26 compared to 43.4% in the prior year period.Increased FY26 revenue guidance to $93 million, representing growth of 55% compared to FY25. “Kestra delivered another strong quarter of financial performance, generating revenue growth of 63% while expanding gross margin to over 52%,” said Brian Webster, President and CEO. “We also continued to execute on several key operational objectives, including rapid growth of the commercial organization, release of compelling primary results from our FDA post-approval study, fortification of our balance sheet with an equity offering, and entrance into a strategic collaboration with Biobeat Technologies. As we progress on our journey to category leadership, our team remains focused on growing the wearable defibrillator market and executing on our commitments to patients and their prescribers.” Third Quarter Fiscal 2026 Financial Results Total revenue was $24.6 million, an increase of 63% compared to the prior year period. 5,462 prescriptions were written for the ASSURE® system, an increase of 58% compared to the prior year period.Revenue growth was driven by higher market share and wearable cardioverter defibrillator (WCD) market expansion. Revenue also benefited from a higher mix of in-network patients and improvements in revenue cycle management capabilities. Gross profit was $12.9 million compared to $6.5 million in the prior year period. Gross margin expanded to 52.6% compared to 43.4% in the prior year period, driven by volume leverage, a higher mix of in-network patients and cost improvement programs. GAAP operating expenses were $47.7 million and included $1.5 million of non-recurring costs. GAAP operating expenses were $27.1 million in the prior year period. Excluding non-recurring costs and share-based compensation expense, operating expenses were $36.1 million in Q3 FY26 compared to $24.8 million in Q3 FY25. The increase was attributable to growth in expenses related to accelerated commercial expansion and public company costs. GAAP net loss and comprehensive loss was $34.2 million compared to GAAP net loss and comprehensive loss of $21.8 million in the prior year period. Adjusted EBITDA* loss was $21.2 million compared to an adjusted EBITDA loss of $16.3 million in the prior year period. Cash and cash equivalents totaled $291 million as of January 31, 2026. Cash and cash equivalents includes the net proceeds Kestra received from an underwritten public offering of 6.9 million common shares, which closed on December 4, 2025. *Adjusted EBITDA is a non-GAAP financial measure. See “Use of Non-GAAP Financial Measures” below for additional information. A reconciliation of Adjusted EBITDA to the most directly comparable GAAP measure is included in this press release. Fiscal Year 2026 Revenue GuidanceKestra is increasing its FY26 revenue guidance to $93 million, which would represent growth of 55% compared to FY25. This compares to prior FY26 revenue guidance of $91 million and initial FY26 guidance of $85 million. Webcast and Conference CallKestra will host a conference call today at 4:30 p.m. ET to discuss financial results. A live and archived webcast of the event will be available in the “Events” section of the investor relations website. Use of Non-GAAP Financial MeasuresThis press release contains certain financial information that is not presented in conformity with U.S. generally accepted accounting principles (“GAAP”), including Adjusted EBITDA. The non-GAAP financial measures are provided as supplemental information to Kestra’s financial measures presented in this press release that are calculated and presented in accordance with GAAP. Adjusted EBITDA, which is calculated as net income (loss), as adjusted to exclude other income/expense (including interest), income tax expense (benefit), depreciation and amortization expense, share-based compensation expense, and non-recurring expenses, is presented because management believes it allows investors to view the Company’s performance in a manner similar to the method used by management to evaluate the Company’s performance for both strategic and annual operating planning. Management believes that in order to properly understand short-term and long-term financial trends, it is helpful for investors to understand the impact of the items excluded from the calculation of Adjusted EBITDA, in addition to considering the Company’s GAAP financial measures. The excluded items vary in frequency and/or impact on our results of operations and management believes that the excluded items are not reflective of our ongoing core business operations and financial condition. Excluding such items allows investors and analysts to compare our operating performance to other companies in our industry and to compare our period-over-period results. The non-GAAP financial measures used by Kestra may not be the same or calculated in the same manner as those used and calculated by other companies. Non-GAAP financial measures have limitations as analytical tools and should not be considered in isolation or as a substitute for Kestra’s financial results prepared and reported in accordance with GAAP. We urge investors to review the reconciliation of these non-GAAP financial measures to the comparable GAAP financial measures included in this press release, and not to rely on any single financial measure to evaluate our business. A reconciliation of Adjusted EBITDA reported in this press release to the most comparable GAAP measure for the respective periods appears in the table captioned “Reconciliation of GAAP Net Income (Loss) to Adjusted EBITDA” later in this release. Within the accompanying financial tables presented, certain columns and rows may not add due to the use of rounded numbers. Forward-Looking StatementsExcept where otherwise noted, the information contained in this press release is as of March 17, 2026. Statements in this press release and on the related teleconference that express a belief, expectation or intention, as well as those that are not historical fact, are forward-looking statements. Except as required by law, the Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise. This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements about, among other topics, our anticipated operating and financial performance, including financial guidance and projections; business plans, strategy, goals and prospects; and expectations for our products. Given their forward-looking nature, these statements involve substantial risks, uncertainties and potentially inaccurate assumptions, and we cannot ensure that any outcome expressed in these forward-looking statements will be realized in whole or in part. You can identify these statements by the fact that they use future dates or use words such as “will,” “may,” “could,” “likely,” “ongoing,” “anticipate,” “estimate,” “expect,” “project,” “intend,” “plan,” “believe,” “assume,” “target,” “forecast,” “guidance,” “goal,” “objective,” “aim,” “seek,” “potential,” “hope” and other words and terms of similar meaning. Kestra’s financial guidance is based on estimates and assumptions that are subject to significant uncertainties. Among the factors that could cause actual results to differ materially from past results and future plans and projected future results are the following: risks related to our limited operating history and history of net losses; our ability to successfully achieve substantial market adoption of our products; competitive pressures; our ability to adapt our manufacturing and production capacities to evolving patterns of demand, governmental actions and customer trends; product defects or complaints and related liability; our ability to obtain and maintain adequate coverage and reimbursement levels for our products; our ability to comply with changing laws and regulatory requirements and resulting costs; our dependence on a limited number of suppliers; risks and uncertainties related to market conditions; and other risks and uncertainties, including those described under the heading “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended April 30, 2025 and other filings filed or to be filed with the U.S. Securities and Exchange Commission (“SEC”). These filings, when made, are available on the Investor Relations section of our website at https://investors.kestramedical.com/ and on the SEC’s website at https://sec.gov/. About KestraKestra Medical Technologies, Ltd. is a leading wearable medical device and digital healthcare company focused on transforming patient outcomes in cardiovascular disease using monitoring and therapeutic intervention technologies that are intuitive, intelligent, and connected. For more information, visit www.kestramedical.com. KESTRA MEDICAL TECHNOLOGIES, LTD. AND SUBSIDIARIESCONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS(in thousands, except share and per share amounts)(unaudited)  Three Months EndedJanuary 31,  Nine Months EndedJanuary 31,   2026  2025  2026  2025              Revenue $24,552  $15,090  $66,488  $42,582 Cost of revenue  11,646   8,543   33,307   26,005 Gross profit  12,906   6,547   33,181   16,577 Operating expenses:            Research and development  4,972   3,353   13,850   10,266 Selling, general and administrative  42,699   23,795   114,728   64,477 Total operating expenses  47,671   27,148   128,578   74,743 Loss from operations  (34,765)  (20,601)  (95,397)  (58,166)Other expense (income):            Interest expense  1,888   1,783   5,702   5,974 Interest income  (2,163)  (628)  (6,125)  (1,543)Other expense (income)  (359)  (15)  (2,299)  73 Net loss before provision for income taxes  (34,131)  (21,741)  (92,675)  (62,670)Provision for income taxes  35   18   102   33 Net loss and comprehensive loss  (34,166)  (21,759)  (92,777)  (62,703)Net loss attributable to non-controlling interest  —   (250)  —   (942)Net loss and comprehensive loss attributable to Kestra Medical Technologies, Ltd.  (34,166)  (21,509)  (92,777)  (61,761)Less: Undeclared preferred stock dividends  —   3,324   —   9,030 Net loss attributable to common shareholders, basic and diluted $(34,166) $(24,833) $(92,777) $(70,791)             Net loss per share attributable to common shareholders, basic and diluted $(0.61) $(1.25) $(1.76) $(3.56)Weighted-average shares of common shares outstanding, basic and diluted  55,848,413   19,885,382   52,843,097   19,885,382  RECONCILIATION OF GAAP NET LOSS AND COMPREHENSIVE LOSS TO ADJUSTED EBITDA(in thousands)(unaudited)  Three Months EndedJanuary 31,  Nine Months EndedJanuary 31,   2026  2025  2026  2025              GAAP Net loss and comprehensive loss $(34,166) $(21,759) $(92,777) $(62,703)Non-GAAP Adjustments:            Interest expense  1,888   1,783   5,702   5,974 Interest income  (2,163)  (628)  (6,125)  (1,543)Other expense (income)  (359)  (15)  (2,299)  73 Provision for income taxes  35   18   102   33 Depreciation expense  1,984   1,888   6,384   6,132 Share-based compensation expense  10,108   459   23,340   1,958 Non-recurring expenses  1,482   1,927   5,396   1,927 Adjusted EBITDA $(21,191) $(16,327) $(60,277) $(48,149) KESTRA MEDICAL TECHNOLOGIES, LTD. AND SUBSIDIARIESCONDENSED CONSOLIDATED BALANCE SHEETS(in thousands, except share and per share amounts)(unaudited)  January 31,  April 30,   2026  2025        Assets      Current assets      Cash and cash equivalents $291,321  $237,595 Accounts receivable, net  12,709   8,081 Disposable medical equipment supplies  6,829   6,572 Prepaid expenses and other current assets  3,204   3,080 Total current assets  314,063   255,328        Right-of-use assets  3,419   2,078 Deposits  1,847   2,021 Restricted cash  334   334 Property and equipment, net  53,799   34,830 Other long-term assets  5,880   1,153 Total assets $379,342  $295,744        Liabilities and Shareholders’ Equity      Current liabilities      Accounts payable $24,023  $23,961 Accrued liabilities  18,898   13,829 Operating lease liabilities, current portion  10   187 Total current liabilities  42,931   37,977        Operating lease liabilities, net of current portion  4,276   3,026 Warrant liabilities  1,745   8,097 Other long-term liabilities  140   140 Long-term debt, net  42,261   41,098 Total liabilities  91,353   90,338        Commitments and contingencies             Shareholders’ equity             Common Shares, $1.00 par value; 100,000,000 shares authorized as of January 31, 2026 and April 30, 2025; 58,349,053 issued and outstanding as of January 31, 2026 and 51,348,656 shares issued and outstanding as of April 30, 2025  58,349   51,349 Additional paid-in capital  842,666   674,306 Accumulated deficit  (613,026)  (520,249)Total shareholders’ equity  287,989   205,406 Total liabilities and shareholders’ equity $379,342  $295,744  KESTRA MEDICAL TECHNOLOGIES, LTD. AND SUBSIDIARIESCONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS(in thousands)(unaudited)  Nine Months EndedJanuary 31,   2026  2025 Cash flows from operating activities      Net loss $(92,777) $(62,703)Adjustments to reconcile net loss to net cash used in operating activities:      Depreciation and amortization  6,384   6,132 Loss on disposal of property and equipment  727   882 Reserve for lost equipment and supplies  1,600   647 Provision for uncollectible accounts receivable  1,515   1,883 Interest paid-in-kind  —   703 Amortization of debt discounts and issuance costs  1,406   1,031 Share-based compensation expense  23,340   1,958 Non-cash lease expense  273   330 Change in fair value of warrant liabilities  (2,297)  — Changes in operating assets and liabilities:      Disposable medical equipment supplies  (466)  (2,823)Prepaid expenses and other current assets  421   (431)Accounts receivable  (6,143)  (7,814)Accounts payable  (647)  3,665 Accrued liabilities  4,192   2,730 Operating lease liabilities  (541)  228 Other long-term assets  30   30 Net cash used in operating activities  (62,983)  (53,552)Cash flows from investing activities      Purchases of property and equipment  (25,228)  (15,547)Deposits for medical rental equipment  (527)  (627)Refund of deposits for medical rental equipment  184   270 Investment in equity security  (5,000)  — Net cash used in investing activities  (30,571)  (15,904)Cash flows from financing activities      Proceeds from issuance of common stock  149,291   — Payment of equity issuance costs  (1,986)  (3,293)Deemed dividend for payments to third party on behalf of shareholder  (25)  (1,648)Proceeds from issuance of redeemable preferred stock  —   103,400 Proceeds from issuance of stock to non-controlling interest  —   17,100 Net cash provided by financing activities  147,280   115,559 Net increase in cash, cash equivalents and restricted cash  53,726   46,103 Cash, cash equivalents and restricted cash      Beginning of period  237,929   8,583 End of period $291,655  $54,686 CONTACT: Investor contact
Neil Bhalodkar
neil.bhalodkar@kestramedical.com

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