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

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

TRAINING IN ENDOVASCULAR SURGERY DURING THE MECHANICAL THROMBECTOMY (MT) INNOVATION BOOM. I was fortunate to have completed ...

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

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

The American College of Cardiology (ACC) reported that the Richard A. and Susan F. Smith Center for Outcomes Research at Beth ...

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

A summary of preclinical evaluation methods for neuroendovascular devices, including in vitro techniques, 3D-printed vascular models, in silico simulations, and in vivo models.

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

A conversation on data from recent trials, lessons learned for future study, definitions and imaging protocols, how treatment can be refined, and more.

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

Dr. Fukaya shares tips for a patient-centered venous disease practice, challenges facing the vascular medicine field, where ...