Other News

Catheter Precision Reports 2025 Results and Updates on Strategic Expansion

Clinical, Commercial and Regulatory Milestones Achieved in 2025 Establish a Strong Foundation in Life Sciences as Revenue Increases 95% Year Over Year Acquisition of Flyte and Strengthened Capital Position Unlock Multi-Segment Growth Strategy with Multiple Near-Term Catalysts FORT MILL, S.C., March 31, 2026 (GLOBE NEWSWIRE) — Catheter Precision, Inc. (NYSE American: VTAK) (“VTAK” or the “Company”), a U.S.-based innovative medical device company focused on electrophysiology products, today announced its financial results and operational update for the fourth quarter and full year ended December 31, 2025 as well as certain other business updates. 2025: Execution Across Clinical, Commercial and Regulatory Milestones Catheter Precision delivered meaningful progress across its core medical device platform in 2025, advancing both commercialization and clinical validation. Operational Highlights CE Mark received for LockeT in April 2025First commercial LockeT sales in EuropeAdded 32 new customers across the VIVO and LockeT platformsFour abstracts accepted at the annual Heart Rhythm Society Meeting Management Commentary “We are pleased with our progress in 2025,” said David A. Jenkins, Chief Executive Officer of Catheter Precision. “We expanded our customer base, advanced commercialization in Europe, and continued to demonstrate the clinical value of both VIVO and LockeT. We believe these achievements position us well as we enter our next phase of growth.” Post-Year-End: Strategic Transformation and Platform Expansion Subsequent to year-end, the Company acquired Fly Flyte, Inc., as disclosed in the Company’s Current Report on Form 8-K filed with the U.S. Securities and Exchange Commission on March 9, 2026. Flyte is a technology-enabled regional air mobility company operating a growing fleet of Cirrus Vision Jets. Focused on high frequency, short haul markets, Flyte is providing a faster, safer, and more efficient alternative to commercial and existing private charter air travel. With certified aircraft, active revenue generating operations and scalable fleet expansion underway, Flyte is seeking to build a disciplined, asset backed aviation infrastructure designed to serve underserved regional markets. This transaction represents a strategic expansion into a large and rapidly growing market, positioning the Company to build a diversified platform spanning both healthcare technology and regional aviation. In parallel, the Company completed financing initiatives designed to strengthen its balance sheet and support the execution of its multi-year growth strategy. Two Platforms. Multiple Catalysts Following the Flyte acquisition, VTAK will operate across two distinct business segments: Medical Device Platform (VIVO & LockeT) Commercial-stage electrophysiology technologiesExpanding global footprint and clinical validationPositioned for continued adoption and growth Aviation Platform (Flyte) Technology-enabled regional air mobility platformActive revenue-generating operations with a scalable fleet modelTargeting high-frequency, short-haul markets with strong demand characteristics Strategic Outlook Management believes the Company is entering 2026 with: Two differentiated growth platforms operating in large addressable marketsStrengthened capital resources to support expansion initiativesMultiple strategic pathways to unlock and optimize shareholder value These include: Scaling the Flyte aviation platform across additional marketsContinued commercialization and clinical adoption of VIVO and LockeTEvaluation of strategic alternatives across business segments to enhance valuation and investor visibility The Company believes these initiatives create a compelling framework for accelerated growth and a potential re-rating as execution milestones are achieved. 2025 Full Year Financial Highlights 2025 Revenue of $819 thousand, a 95% increase over 2024 Revenue of $420 thousand.2025 Gross Margin of 92.3% compared with 90.0% in 2024.Net Loss of $17.2 million of which $7.8 million was non-cash compared with $16.6 million of which $7.5 million was non-cash in 2024.1 2025 Fourth Quarter Financial Highlights Revenue increased 60% to $238 thousand compared to fourth quarter of 2024 Revenue of $148 thousand.Gross margin of 91.6% compared to 92.6% in Q4 2024.Net Loss of $5.3 million of which $3.5 million was non-cash compared with $5.6 million of which $3.1 million was non-cash in 2024.1 1. Non-cash calculations are non-GAAP measures described in the section titled “Non-GAAP Financial Measures” below and reconciled to the most directly comparable GAAP measures at the end of this release. About Catheter Precision Catheter Precision is an innovative U.S.-based medical device company bringing new solutions to market to improve the treatment of cardiac arrhythmias. It is focused on developing groundbreaking technology for electrophysiology procedures by collaborating with physicians and continuously advancing its products. About VIVO Catheter Precision’s VIVO™ (View Into Ventricular Onset), is a non-invasive 3D imaging system that enables physicians to identify the origin of ventricular arrhythmias pre-procedure, thereby streamlining workflow and reducing procedure time. VIVO has received marketing clearance from the U.S. FDA and has the CE mark. About LockeT Catheter Precision’s LockeT is a suture retention device intended to assist in hemostasis after percutaneous venous punctures. LockeT is a Class 1 device registered with the FDA. About Flyte Flyte is a technology-enabled Regional Air Mobility Company operating a growing fleet of Cirrus Vision Jets. Focused on high frequency, short haul markets, Flyte provides a faster, safer, and more efficient alternative to commercial and existing private charter air travel. Flight operations are conducted through Flyte’s wholly-owned subsidiary, Ponderosa Air, LLC, an FAA certified Part 135 air carrier. With certified aircraft, active revenue generating operations, and scalable fleet expansion underway, Flyte is seeking to building disciplined, asset backed aviation infrastructure designed to serve underserved regional markets. For more information, visit www.flyte.travel Additional Information This release and all other releases from Catheter Precision, Inc. are limited in their entirety by other information filed with the U.S. Securities and Exchange Commission (the “SEC”) including, but not limited to, our latest Form 10-K, Form 10-Q’s, and Form 8-K’s, and should be read in conjunction with those filings. Non-GAAP Financial Measures Certain Non-GAAP financial measures are included in this press release. In the calculation of these measures, the Company excludes certain items, such as amortization of intangible assets, stock-based compensation, tax impact of adjustments, other unusual items and discrete items impacting income tax expense. The Company believes that excluding such items provides investors and management with a representation of the Company’s core operating performance and with information useful in assessing its prospects for the future and underlying trends in the Company’s operating expenditures and continuing operations. Management uses such Non-GAAP measures to evaluate financial results and manage operations. The release and the attachments to this release provide a reconciliation of each of the Non-GAAP measures referred to in this release to the most directly comparable GAAP measure. The Non-GAAP financial measures are not meant to be considered a substitute for the corresponding GAAP financial statements and investors should evaluate them carefully. These Non-GAAP financial measures may differ materially from the Non-GAAP financial measures used by other companies. Forward Looking Statements This communication contains forward-looking statements. Forward-looking statements can be identified by words such as “believe,” “anticipate,” “may,” “might,” “can,” “could,” “continue,” “depends,” “expect,” “expand,” “forecast,” “intend,” “predict,” “plan,” “rely,” “should,” “will,” “may,” “seek,” or the negative of these terms and other similar expressions, although not all forward-looking statements contain these words. These forward-looking statements are subject to the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. Forward-looking statements contained in this press release include, but are not limited to, statements regarding the following: our belief that our VIVO and Locket achievements position us well as we enter our next phase of growth, our belief the Company in entering into 2026 with two differentiated growth platforms operating in large addressable markets, strengthened capital resources to support expansion initiatives and multiple strategic pathways to unlock and optimize shareholder value and our belief the Company’s current initiatives create a compelling framework for accelerated growth and a potential re-rating as execution milestones are achieved . The Company’s expectations and beliefs regarding these matters may not materialize. Actual outcomes and results may differ materially from those contemplated by these forward-looking statements as a result of uncertainties, risks and changes in circumstances, including but not limited to risks and uncertainties included under the caption “Risk Factors” in the Company’s 2025 Form 10-K filed with the SEC and available at www.sec.gov. These risks and uncertainties include, but aren’t limited to, that the results of anticipated trials may not turn out as we currently expect and future trials may not occur on the time tables we expect or may be more costly than anticipated, we do not have sufficient liquidity to fund our operations through fiscal year 2026 unless we are able to obtain additional financing or enter into a strategic transaction that would provide additional liquidity, our ability to implement and integrate our new Flyte acquisition and strategy, we will not be able to reach profitability unless we are able to achieve our product expansion and growth goals, our research and development and commercialization efforts may depend on entering into agreements with corporate collaborators, we have entered into joint marketing agreements with respect to our products, and may enter into additional joint marketing agreements, that will reduce our revenues from product sales, royalty agreements with respect to our LockeT device will reduce any future profits from this product, if we experience significant disruptions in our information technology systems, our business may be adversely affected, litigation and other legal proceedings may adversely affect our business, if we make acquisitions or divestitures, we could encounter difficulties that harm our business, failure to attract and retain sufficient qualified personnel could also impede our growth, failure to maintain effective internal controls could cause our investors to lose confidence in us and adversely affect the market price of our common stock, , we may not be able to accurately report our financial results or prevent fraud, our revenues may depend on our customers’ receipt of adequate reimbursement from private insurers and government sponsored healthcare programs, we may be unable to compete successfully with companies in our highly competitive industry, many of whom have substantially greater resources than we do, our future operating results depend upon our ability to obtain components in sufficient quantities on commercially reasonable terms or according to schedules, prices, quality and volumes that are acceptable to us, and suppliers may fail to deliver components, or we may be unable to manage these components effectively or obtain these components on such terms, if hospitals, physicians and patients do not accept our current and future products or if the market for indications for which any product candidate is approved is smaller than expected, we may be unable to generate significant revenue, if any, our medical device operations are subject to pervasive and continuing FDA regulatory requirements, our products may be subject to additional recalls, revocations or suspensions after receiving FDA or foreign approval or clearance, which could divert managerial and financial resources, harm our reputation, and adversely affect our business, changes in trade policies among the U.S. and other countries, in particular the imposition of new or higher tariffs, could place pressure on our average selling prices as our customers seek to offset the impact of increased tariffs on their own products, increased tariffs or the imposition of other barriers to international trade could have a material adverse effect on our revenues and operating results. The risks and uncertainties described above may be amplified by supply chain disruptions from the Ukraine war or Iran conflict and otherwise, and ongoing volatility in the stock markets and the U.S. economy in general. The forward-looking statements included in this communication are made only as of the date hereof. The Company assumes no obligation and does not intend to update these forward-looking statements, except as required by law. CONTACTS: At the CompanyInvestor Relations973-691-2000IR@catheterprecision.com RECONCILIATION OF SELECTED GAAP MEASURES TO NON-GAAP MEASURES(in thousands)CALCULATION OF NON-CASH NUMBERS  2025 2024 Net loss-$17,695-$16,643     non-cash add backs:   intangible asset impairment$6,995 – loss on debt extinguishment$3,260 – depreciation & amortization$2,115$2,109 stock-based compensation$338$54 change in fair value of royalties payable-$5,709$2,239 deferred income tax (benefit)-$1,810$3,141 acquired in-process R&D$1,967 – other$607 – total adjusted net loss (non-GAAP)$7,763$7,543   Q4 2025Q4 2024 Net loss-$5,336-$5,628     non-cash add backs:   intangible asset impairment$6,995- loss on debt extinguishment$3,260- depreciation & amortization$527$531 stock-based compensation$79$18 change in fair value of royaltiespayable-$7,813-$584 deferred income tax (benefit)-$214$3,141 acquired in-process R&D$0$0 other$697$0 total adjusted net loss (non-GAAP)$3,531$3,106 

SS Innovations Expands Global Opportunity with Regulatory Approval of the SSi Mantra Surgical Robotic System in Colombia, Oman, Sri Lanka and Kenya

FORT LAUDERDALE, Fla., March 30, 2026 (GLOBE NEWSWIRE) — SS Innovations International, Inc. (the “Company” or “SS Innovations”) (Nasdaq: SSII), a developer of innovative surgical robotic technologies dedicated to making robotic surgery affordable and accessible to a global population, today announced that the Company has received regulatory approval for the SSi Mantra surgical robotic system (the “SSi Mantra”), for multiple indications in Colombia, Oman, Sri Lanka and Kenya. The Company received regulatory approval for the SSi Mantra from the Instituto Nacional de Vigilancia de Medicamentos y Alimentos (“INVIMA”) in Colombia in November 2025, from the Directorate General of Pharmaceutical Affairs and Drug Control (“DGPA&DC”) in Oman in November 2025, from the National Medicines Regulatory Authority (“NMRA”) in Sri Lanka in January 2026, and from the Pharmacy and Poisons Board (“PPB”) in Kenya in January 2026. SS Innovations believes that it is favorably positioned to address these underpenetrated markets given the SSi Mantra’s cost advantages combined with its advanced technology, differentiated features, ease of training, and user-friendliness. Dr. Sudhir Srivastava, Chairman of the Board and Chief Executive Officer of SS Innovations, commented, “We continue to expand SS Innovations’ global opportunity with an eye on democratizing access to cutting-edge robotic surgery for patients in underserved regions of the world. Over the past few months, our advanced, cost-efficient SSi Mantra surgical robotic system has received regulatory approval in Colombia, Oman, Sri Lanka, and Kenya. We are committed to decentralizing excellence in surgical robotic care in these new jurisdictions, among others, while pursuing the established United States and Europe Union markets. We anticipate that the U.S. Food and Drug Administration will complete its review of our 510(k) premarket notification for the SSi Mantra by mid-2026. Separately, we continue along the pathway towards a European Union CE marking certification for the SSi Mantra, which we believe we can obtain in 2026.” To date, the SSi Mantra has been granted regulatory approval in eleven countries, including India and the following: Colombia Oman Ecuador Philippines Guatemala Sri Lanka Indonesia Ukraine Kenya United Arab Emirates    As of December 31, 2025, the SSi Mantra cumulative installed base totaled 168 across ten countries and cumulative surgeries reached 7,885, including 390 cardiac procedures and 121 pediatric surgeries. To date, more than 150 telesurgeries have been performed with the SSi Mantra. About SS Innovations SS Innovations International, Inc. (Nasdaq: SSII) develops innovative surgical robotic technologies with a vision to make the benefits of robotic surgery affordable and accessible to a larger segment of the global population. The Company’s product range includes its proprietary “SSi Mantra” surgical robotic system and its comprehensive suite of “SSi Mudra” surgical instruments, which support a variety of robotic surgical procedures including cardiac surgery. An American company headquartered in India, SS Innovations plans to expand the global presence of its technologically advanced, user-friendly, and cost-effective surgical robotic solutions. Visit the Company’s website at ssinnovations.com or LinkedIn for more information and updates. About the SSi Mantra The SSi Mantra surgical robotic system is a user-friendly, modular, multi-arm system with advanced technology features, including: 3 to 5 modular robotic arms, an open-faced ergonomic surgeon command center, a large 3D 4K monitor, a touch panel monitor for all patient related information display, a virtual real-time image of the robotic patient side arm carts, and the ability for superimposition of 3D models of diagnostic imaging. The optional SSi MantrAsana Tele Surgeon Console is a portable, compact alternative to the SSi Mantra’s standard surgeon command center that provides equivalent control functionality while enabling enhanced portability, ergonomic flexibility, and telesurgery capability. The SSi Mantra utilizes over 40 different types of robotic endo-surgical instruments to support different specialties, including cardiac surgery, and 5mm instruments for the pediatric population and ENT surgeries. A vision cart provides the table-side team with the same magnified 3D 4K view as the surgeon to provide better safety and efficiency. The SSi Mantra has been clinically validated in India in more than 100 different types of surgical procedures. Forward Looking StatementsThis press release may contain statements that are not historical facts and are considered forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. The words “anticipate,” “assume,” “believe,” “estimate,” “expect,” “will,” “intend,” “may,” “plan,” “project,” “should,” “could,” “seek,” “designed,” “potential,” “forecast,” “target,” “objective,” “goal,” or the negatives of such terms or other similar expressions to identify such forward-looking statements. These statements relate to future events or SS Innovations’ future financial performance and involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance, or achievements to be materially different from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Investor Contact:The Equity GroupKalle Ahl, CFAT: (303) 953-9878kahl@theequitygroup.com Devin Sullivan, Managing Director T: (212) 836-9608dsullivan@theequitygroup.com Media Contact:RooneyPartners LLCKate BarretteT: (212) 223-0561kbarrette@rooneypartners.com

Emboline Announces Positive Pivotal PROTECT H2H Trial Results for Emboliner® Presented as a Late-Breaking Clinical Trial at ACC 2026

Randomized IDE study met all primary and secondary safety and efficacy endpoints and demonstrated superior debris capture and significantly higher technical success versus the leading embolic protection control device in TAVR SANTA CRUZ, Calif., March 30, 2026 /PRNewswire/ — Emboline,…

Medical AI Named First-Ever Recipient of ACC Global Digital Health Award at American College of Cardiology Annual Scientific Session

AI platform recognized for real-world clinical impact through analysis of raw 12-lead ECG data, enabling earlier detection of multiple cardiovascular diseasesNEW ORLEANS, March 29, 2026 (GLOBE NEWSWIRE) — Medical AI, a company specializing in artificial intelligence-enabled electrocardiogram (ECG) solutions for cardiovascular disease detection and monitoring, today announced that it has received the inaugural Global Digital Health Award at the American College of Cardiology’s (ACC) Annual Scientific Session. The award was presented by Dr. Ami Bhatt, Chief Innovation Officer of the ACC, during the conference’s Future Hub Theater session, which highlights breakthrough technologies shaping the future of cardiovascular medicine. Medical AI was selected for its AI platform that analyzes raw data from standard 12-lead electrocardiograms, enabling clinicians to detect multiple cardiovascular conditions earlier and more accurately, including heart failure, myocardial infarction, and aortic stenosis. The award recognizes organizations outside the United States that are demonstrating measurable real-world impact through digital health innovation, including artificial intelligence, data analytics, and connected health technologies that advance cardiovascular care. “Receiving the first Global Digital Health Award from the American College of Cardiology is a tremendous honor,” said Joon-myoung Kwon, Chief Executive Officer of Medical AI. “Our goal has always been to translate advances in artificial intelligence into practical tools that help clinicians detect cardiovascular disease earlier and manage patients more effectively. This recognition underscores the growing importance of AI-driven diagnostics in improving patient outcomes around the world.” “ACC is a supporter of emerging technologies that help to further the College’s mission to transform cardiovascular care and improve heart health for all,” Dr. Bhatt said. “Medical AI’s groundbreaking work in AI to improve the cardiovascular field and lives of patients is the impactful solution we aimed to recognize with the Global Digital Health Award. Congratulations to Medical AI for this recognition.” Medical AI’s technology analyzes raw waveform data from standard 12-lead electrocardiograms to enable earlier detection and monitoring of a wide range of cardiovascular conditions, helping clinicians identify disease earlier in routine care settings. The company’s solutions have demonstrated strong real-world clinical adoption, currently deployed in 250 hospitals and health screening centers worldwide. Following national reimbursement approval in 2023, the technology is now used to evaluate approximately 220,000 patients per month on a reimbursed basis. The company’s technology platform is supported by a growing body of clinical research, including more than 70 publications in SCI-indexed journals, with findings presented in Late-Breaking Research at the 2025 European Society of Cardiology Heart Failure Congress. Medical AI has received regulatory approvals in six countries, including CE marking, and is currently pursuing U.S. Food and Drug Administration clearance, expected later this year. Dr. Hak Seung Lee, Chief Medical Officer of Medical AI, who accepted the award on behalf of the company, said, “Artificial intelligence has the potential to fundamentally reshape how cardiovascular disease is detected and managed. By extracting deeper insights from standard ECG tests, we can help physicians identify signs of cardiovascular disease earlier and make more informed decisions in everyday clinical settings. We are pleased that ACC has recognized the importance of the work we are doing with this award.” The American College of Cardiology Annual Scientific Session is one of the world’s leading gatherings focused on cardiovascular medicine, bringing together cardiologists, researchers, and healthcare innovators from across the globe to share the latest advances in science, technology, and clinical practice. About Medical AI Medical AI is a digital health company focused on developing artificial intelligence technologies that support clinicians in the diagnosis and management of cardiovascular disease. The company specializes in AI-enabled electrocardiogram analysis solutions that leverage raw ECG data to enable earlier detection of multiple cardiovascular conditions and support more accurate clinical decision-making at scale across diverse care settings. The company’s technology platform is supported by a growing body of clinical research, including more than 70 SCI-indexed publications.   Medical AI has obtained regulatory approvals in six countries, including CE marking, and is currently pursuing U.S. Food and Drug Administration clearance, expected in 2026. Medical AI is headquartered in Seoul. For more information, visit www.medicalai.com. CONTACT: U.S. Media Contact:
Eliza Schleifstein
ES Media
+1 917 763-8106
eliza@schleifsteinpr.com

REPATHA® CUTS RISK OF FIRST MAJOR CARDIOVASCULAR EVENTS BY 31% IN HIGH-RISK PATIENTS WITHOUT KNOWN SIGNIFICANT ATHEROSCLEROSIS

Repatha is the Only PCSK9 Inhibitor to Significantly Reduce the Risk of First CV Events in High-Risk Primary Prevention VESALIUS-CV Subgroup Findings Reinforce Benefit of Earlier Initiation of Repatha in High-Risk Patients, with Median 44 mg/dL LDL-C Achieved THOUSAND OAKS, Calif., March…

CHAMPION-AF study of the WATCHMAN FLX™ Left Atrial Appendage Closure Device as a first-line therapy for stroke risk reduction meets all primary and secondary safety and efficacy endpoints

Data highlights the WATCHMAN FLX device provided statistically superior protection from bleeding, demonstrated similar efficacy compared to blood thinners in patients with non-valvular atrial fibrillation Late-breaking findings presented at ACC.26 and simultaneously published in The New…