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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…

HI-PEITHO trial demonstrates Boston Scientific EKOS™ Endovascular System is superior to standard of care for treatment of acute pulmonary embolism

Global randomized trial demonstrated statistically significant reduction in clinical event rates in patients with intermediate-risk PE when treated with the EKOS device plus anticoagulation vs. anticoagulation alone Late breaking findings presented at ACC.26 and simultaneously published…

Adagio Medical Reports Fourth Quarter and Full Year 2025 Results

LAGUNA HILLS, Calif.–(BUSINESS WIRE)–Adagio Medical Holdings, Inc. (Nasdaq: ADGM) (“Adagio” or “the Company”), a leading innovator in catheter ablation technologies for the treatment of cardiac arrhythmias, today announced financial results for the fourth quarter ended December 31, 2025. Fourth Quarter and Recent Business Highlights: Announced the peer-reviewed publication in Circulation: Arrythmia and Electrophysiology, highlighting results from the U.S. Early Feasibility Study evaluating ul

FDA clears Philips AI solution that provides real-time guidance during complex minimally invasive heart valve repair

Physician using DeviceGuide with EchoNavigator 5

Physician using DeviceGuide with EchoNavigator 5

Philips DeviceGuide with EchoNavigator 5 Screen

Philips DeviceGuide with EchoNavigator 5 Screen

DeviceGuide with EchoNavigator 5

DeviceGuide with EchoNavigator 5

March 26, 2026 Philips DeviceGuide uses AI to track and visualize mitral valve repair devices [1] in real time during minimally invasive procedures, supporting treatment [2]DeviceGuide integrates with Philips Azurion image-guided therapy platform that combines imaging, real-time data and intelligent software within a unified workflow to support more consistent, efficient and confidently guided minimally invasive procedures Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for EchoNavigator R5.0 with DeviceGuide, an AI-powered software solution that assists physicians during one of interventional cardiology’s most technically demanding procedures – repairing leaking mitral valves through a minimally invasive approach. DeviceGuide was developed in close collaboration with Edwards Lifesciences, the global leader in structural heart innovation, aligning Philips’ imaging and AI expertise with Edwards’ expertise in valvular heart therapy development. Together, the companies have innovated image guidance of the mitral transcatheter edge-to-edge repair (M-TEER) workflow to make these complex minimally invasive heart valve repair procedures more intuitive and streamlined. DeviceGuide will be showcased at the American College of Cardiology (ACC) 2026 meeting in New Orleans, one of the world’s leading forums for cardiovascular innovation. Transforming treatment for a common heart conditionA leaking mitral valve, known as mitral regurgitation (MR), affects more than 35 million adults worldwide and over 2 million in the U.S. [3, 4]. Minimally invasive transcatheter techniques such as M-TEER offer an alternative to open heart surgery in selective patient populations. During M-TEER procedures, physicians make a small skin incision to access a vein which allows the introduction of a catheter to the heart to deliver a repair device to the diseased mitral valve. Because the mitral valve is inherently a complex and heterogeneous structure, transcatheter repair of the valve requires experienced physicians positioning the device delivery system, and physicians guiding the placement of the device. In guiding and positioning the repair device, the intraprocedural heart team must interpret both X-ray and ultrasound images on multiple screens, communicate and coordinate movements between two operators, and make precise adjustments to grasp the moving valve leaflets and then confirm the result in real time. The process demands accuracy, coordination, and experience from the entire team – and this is where DeviceGuide can help with navigation guidance. How AI assists inside the beating heartBuilt on Philips’ EchoNavigator echo-fluoro fusion technology, which combines live echocardiography images from Philips EPIQ CVxi cardiovascular platform with live X-ray images from Philips Azurion image-guided therapy system, DeviceGuide brings real-time AI guidance directly into the procedure room. The software’s AI algorithm automatically tracks and visualizes the Edwards PASCAL Ace mitral valve repair device, combining live ultrasound and X-ray images into a single, integrated view. This helps clinicians navigate and position the device with greater clarity and confidence. “The AI software serves as an assistive tool; the physician always remains in control. This isn’t about replacing expertise – it’s about amplifying it,” explains Dr. Atul Gupta, Chief Medical Officer Diagnosis & Treatment at Philips. “By embedding AI into the procedure, DeviceGuide gives physicians an extra pair of eyes, helping them treat more patients safely and confidently.” Collaboration with clinical partnersIn developing DeviceGuide, Philips and Edwards worked closely with investigational sites in Europe and the U.S., including a team at the Structural Heart and Valve Center at NewYork-Presbyterian/Columbia University Irving Medical Center, led by interventional cardiologist Susheel Kumar Kodali, MD, director, and Rebecca T. Hahn, MD, director of interventional echocardiography.“In helping to guide mitral repair procedures, one of my roles as an echocardiographer is to help the interventional cardiologist understand the complex anatomy of the valve which will determine the orientation, trajectory and position of the repair device relative to the target and the surrounding structures,” said Dr. Hahn. “Since AI auto-aligns imaging to the device in real time and continuously informs the interventionalist about the location of the device in space on the imaging screen, it minimizes unnecessary repositioning of the imaging window, streamlines procedural guidance and may improve the precision of device implantation.” “DeviceGuide provides me with a visual overlay, trajectory line and orientation line of the therapy device in both live 3D echo and fluoroscopic images during mitral valve repair procedures,” said Dr. Kodali. “Having a single, intuitive presentation of real-time target, orientation and auto device-aligned views simplifies this procedure and improves team communication.” Supporting teams in real time“Structural heart procedures are among the fastest-growing areas in cardiology, and also among the most complex,” said Mark Stoffels, Business Leader, Image Guided Therapy Systems at Philips. “By assisting physicians with real-time visualization and navigation inside the beating heart, DeviceGuide helps them manage that complexity, and perform procedures more confidently, with the ultimate goal to treat more patients effectively. It fits seamlessly into cath-lab workflows and gives the entire team a shared view of the procedure, improving coordination and confidence.” Part of Philips’ connected cardiology ecosystemDeviceGuide extends Philips’ connected cardiology portfolio that helps physicians care for heart patients from diagnosis through recovery. It also represents a step toward Philips’ vision of the AI-powered cath lab of the future where imaging, devices, and real-time data are intelligently connected to reduce procedural complexity and improve consistency. In hospitals, Philips systems already bring together ultrasound, X-ray, and real-time data into a unified workflow to guide minimally invasive procedures. Building on this foundation, intelligent software solutions such as DeviceGuide help care teams navigate complex structural heart interventions with greater clarity and coordination, serving as an assistive “copilot” in the procedure room.After treatment, Philips connected monitoring tools extend care beyond the cath lab, helping care teams detect complications early and support recovery. Together, these innovations create a connected cardiology ecosystem that helps care teams diagnose earlier, treat less invasively, improve procedural efficiency, and support recovery – improving outcomes and experiences for heart patients everywhere. AvailabilityDeviceGuide enabled by EchoNavigator is FDA 510(k) cleared in the United States. Commercial availability is subject to market release and applicable regulatory requirements. DeviceGuide is currently intended for use with the Edwards PASCAL Ace Mitral Valve Repair System. Availability outside the U.S. varies by country and regulatory status. A recent first-in-human publication in JACC: Case Reports describes early clinical experience using DeviceGuide for AI-supported imaging guidance during mitral transcatheter edge-to-edge repair procedures. Read more on how Philips DeviceGuide works here. Philips DeviceGuide enabled by EchoNavigator R5 is not available for sale or use in all countries. Its availability is subject to local regulatory clearance and market release. Please contact your Philips representative for details on product availability in your region. Dr. Hahn reports Institutional funding to Columbia University and/or the Cardiovascular Research Foundation from Philips North America LLC, and from Edwards Lifesciences Corporation.Dr. Kodali discloses consulting payments from Philips North America LLC and reports Institutional funding to Columbia University and/or the Cardiovascular Research Foundation from Edwards Lifesciences Corporation. REFERENCES:[1] DeviceGuide is currently intended for use only with the Mitral TEER Therapy Device (Edwards PASCAL Ace); Hahn RT, Biaggi P, Corti R et al. Mitral Transcatheter Edge-to-Edge Repair Using Novel Augmented Imaging Software. JACC: Case Reports 2025;30:106160.[2] DeviceGuide assists physicians in visualizing and navigating the repair device within the heart. It supports, but does not perform, the therapeutic procedure itself; Biaggi P, Corti R, Gaemperli O et al. Artificial intelligence based fusion imaging streamlining mitral transcatheter edge-to-edge repair. European Heart Journal – Imaging Methods and Practice 2026;4.[3] MDPI[4] CDC For further information, please contact: Joost MalthaPhilips Global External RelationsTel.: +31 6 1055816E-mail: joost.maltha@philips.com Avi DinesPhilips North AmericaTel: +1 781 690 3814E-mail: avi.dines@philips.com About Royal Philips  Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people’s health and well-being through meaningful innovation. Philips’ patient- and people-centric innovation leverages advanced technology and deep clinical and consumer insights to deliver personal health solutions for consumers and professional health solutions for healthcare providers and their patients in the hospital and the home. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, ultrasound, image-guided therapy, monitoring and enterprise informatics, as well as in personal health. Philips generated 2025 sales of EUR 18 billion and employs approximately 64,800 employees with sales and services in more than 100 countries. News about Philips can be found at www.philips.com/newscenter.

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Physician using DeviceGuide with EchoNavigator 5

Philips DeviceGuide with EchoNavigator 5 Screen

DeviceGuide with EchoNavigator 5