Anaconda Biomed, SL, announced that it has received CE Mark certification for its ANA5 advanced neurovascular access funnel ...

Crossroads Neurovascular, Inc. announced FDA 510(k) clearance for the company’s Path balloon guide catheter (BGC) for neurov ...

Penumbra, Inc. announced the completion of enrollment in the pivotal STORM-PE prospective, multicenter, randomized controlled tria ...

Inquis Medical announced that its Aventus mechanical thrombectomy system has received FDA 510(k) clearance for an expanded ...

InspireMD, Inc. recently announced it has received CE Mark approval under the European Medical Device Regulation (EU MDR) for ...

With a distribution agreement in place and an option to acquire Contego Medical, Medtronic’s peripheral vascular division ki ...

Nectero Medical announced that the American Medical Association’s CPT Editorial Panel has approved two Category III CPT code ...

Viz.ai announced it has received FDA 510(k) clearance for Viz Subdural Plus, a comprehensive solution for quantifying the ...

HistoSonics, Inc. recently announced the completion of patient enrollment in the #HOPE4KIDNEY pivotal trial of its Edison histotri ...

Medtronic announced the treatment of the first patient in the United States in the Global SYMPLICITY Registry (GSR) DEFINE. The cl ...

June 11, 2025—enVVeno Medical Corporation recently announced interim 2-year follow-up data on 42 of 75 patients in the VenoValve United States p ...