Okami Medical announced its Sendero Max delivery catheter has received 510(k) clearance from the FDA. The Sendero Max ...
Imperative Care, Inc. announced FDA 510(k) clearance of the 82 cm version of its Symphony 16-F catheter for the treatment of veno ...
Merit Medical Systems, Inc. announced the publication of the 6-month results from the randomized arm of the WAVE trial of arterio ...
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 ...
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 ...
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 ...
Fogarty Innovation and the Linda and Mike Mussallem Foundation announced the call for nominations for the inaugural Thomas J.
Route 92 Medical, Inc. announced the results of a multicenter study evaluating the utility of the company’s Monopoint venou ...
T45 Labs announced the close of its $25 million T45 Fund I. The fund will advance and fuel development and clinical research prog ...
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