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 ...

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

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

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

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

Perfuze, an Ireland-based developer of catheter-based aspiration technology for the treatment of acute ischemic stroke, ...

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

T45 Labs announced the close of its $25 million T45 Fund I. The fund will advance and fuel development and clinical research prog ...

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

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

Route 92 Medical, Inc. announced the results of a multicenter study evaluating the utility of the company’s Monopoint venou ...