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 ...

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

Penumbra, Inc. announced that data from the THRIVE study demonstrated the potential of the company’s computer assisted vacuum ...

Penumbra, Inc. announced the FDA clearance and launch of the Ruby XL system, part of the company’s Ruby portfolio of peripher ...

Teleflex Manta Vascular Closure Device Bioresorbable implant Following the use of 10–20 F device or sheaths (12–25 F OD) 0.035 Indicated for closure of femoral artery access sites while reducing time ...

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Front Line Medical Technologies Inc. COBRA-OS REBOA (large vessel balloon occlusion device; 4-F; 25-mm-diameter balloon; guidewire-free) Aortic Temporary occlusion of large blood vessels and/or ...

Front Line Medical Technologies Inc. COBRA-OS REBOA (large vessel balloon occlusion device; 4-F; 25-mm diameter-balloon; guidewire-free) Distal Intended for temporary occlusion of large vessels ...