Nine leading medical societies have issued a call for updated safety standards in fluoroscopy laboratories, where clinicians ...

Abbott announced that its transcatheter Esprit below-the-knee (BTK) everolimus-eluting resorbable scaffold system has been ...

Perfuze, an Ireland-based developer of catheters for interventional stroke care, announced it has received FDA 510(k) ...

Boston Scientific announced FDA clearance for the “Any Day Dosing” feature on the company’s TheraSphere 360 ytt ...

Peijia Medical, a China-based domestic medical device company focused on transcatheter valve therapeutics and neurovascular inter ...

March 19, 2026—iVascular announced 1-year results from the BARISTA clinical trial, which is evaluating the safety and efficacy of the company&rs ...

March 18, 2026—iVascular announced 3-year follow-up results from the LUMIFOLLOW registry, a large real-world study evaluating ...

Terumo Aortic announced that the FDA has granted Breakthrough Device designation for the company’s fenestrated Treo abdomin ...

Imperative Care, Inc., a developer of treatments for thromboembolic disease, announced the closing of a $100 million ...

Thrombolex, Inc., a commercial-stage developer of a differentiated pharmacomechanical lysis platform for the treatment of ...

Three-year outcomes from the PERFORMANCE II trial studying the Neuroguard Integrated Embolic Protection (IEP) 3-in-1 Carotid Sten ...

Cook Medical announced it has selected Indiana University (IU) in Indianapolis, Indiana, as one of the first Interventional ...