Coronary/Structural Heart

First patient treated in Medtronic multi-organ SPYRAL GEMINI Pilot study

Medtronic advances pipeline with update on multi-organ denervation study and additional data recently presented at EuroPCR 2025   Medtronic, a global leader in healthcare technology, today announced that it has treated the first patient in its SPYRAL GEMINI Pilot program (including ‘OFF MED’ and ‘ON MED’ studies).* The first patient […]

CorFlow Therapeutics Announces FDA Approval of the MOCA-II IDE Pivotal Trial to Validate a Novel Heart Attack Care Technology

BAAR, Switzerland–(BUSINESS WIRE)–CorFlow Therapeutics AG (CorFlow), a pioneering company in the field of cardiac care targeting microvascular disease, today announced that the U.S. Food & Drug Administration (FDA) has approved the company’s technology for investigational device exemption (IDE), which allows the pivotal clinical trial to begin at U.S. hospitals. CorFlow will now […]

Lifeforce and Toku Combine AI Retinal Scans with the World’s Largest Longevity-Medicine Platform to Take Steps to Slow Aging and Reduce Cardiovascular Risk

SANTA MONICA, Calif., July 7, 2025 /PRNewswire/ — Lifeforce, the world’s largest longevity medicine platform, and Toku, a health technology company using AI to translate a single retinal image into real-time biological age and cardiovascular risk scores, have announced a nationwide…

CMS Recognizes Eko Health’s AI-Powered Heart Disease Detection in OPPS July 2025 Update, Establishing Payment Rate for SENSORA®

CPT Code for AI-Enabled Cardiac Analysis, Issued by the American Medical Association (AMA), Also Takes Effect July 1, 2025 SAN FRANCISCO, July 1, 2025 /PRNewswire/ — Eko Health, a leader in AI-powered cardiac and pulmonary care, announced a major step forward in expanding access to early…

Mesoblast and FDA Align on Key Items for Revascor® Biologic License Application in Ischemic Heart Failure

NEW YORK, June 30, 2025 (GLOBE NEWSWIRE) — Mesoblast (Nasdaq:MESO; ASX:MSB), global leader in allogeneic cellular medicines for inflammatory diseases, today announced alignment with the United States Food and Drug Administration (FDA) on items required for filing a Biologics License Application (BLA) for Revascor® (rexlemestrocel-L) in the treatment of patients with ischemic heart failure with reduced ejection fraction (HFrEF) and inflammation.