Investigators seeking to compare real-world outcomes with drug-eluting stents (DES) in symptomatic femoropopliteal lesions ...

SonoVascular, Inc. recently announced it has successfully completed an initial set of eight cases in patients with deep vein thro ...

Merit Medical Systems, Inc. announced the publication of the 6-month results from the randomized arm of the WAVE trial of arterio ...

Okami Medical announced its Sendero Max delivery catheter has received 510(k) clearance from the FDA. The Sendero Max ...

Evident Vascular, Inc., developer of an intravascular ultrasound (IVUS) platform powered by artificial intelligence and designed ...

Endologix LLC announced it has reached a milestone of 1,000 patients who have been treated with percutaneous transmural ...

Mark H. Wholey, MD, FSIR, a founding member of the Society of Interventional Radiology (SIR) and the society’s president from ...

The FDA announced that Medtronic initiated a device recall and correction for embolization devices. The FDA has identified ...

Imperative Care, Inc. announced FDA 510(k) clearance of the 82 cm version of its Symphony 16-F catheter for the treatment of veno ...

The American Heart Association (AHA) announced the publication of a new scientific statement that summarizes differences in diagn ...

Ostial Corporation, a California-based medical device company focused on aorto-ostial interventions, announced its new ...

VentureMed Group, Inc., a medical device company focused on arteriovenous access and peripheral arterial disease, recently ...