Embolization, Inc., a medical device company based in Boulder, Colorado, announced its nitinol-enhanced device (NED) has ...

StentIt, a Netherlands-based developer of stents with regenerative properties, announced the successful implantation of its resorb ...

Endovascular Engineering, Inc. (E2) announced the completion of patient enrollment in the pivotal cohort of the ENGULF investigati ...

Thrombolex, Inc., a developer of treatments for arterial and venous thromboembolic diseases, announced the publication of the resu ...

AngioDynamics, Inc. announced first patient enrollment in the RECOVER-AV clinical trial. The prospective, multicenter, multination ...

Gore & Associates announced that the company’s TAG thoracic branch endoprosthesis (TBE) has received FDA approval for us ...

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

Vivasure Medical announced that it has received European CE Mark approval for an expanded indication for its fully bioresorbable, ...

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

InspireMD, Inc. announced that the FDA has granted premarket approval of the company’s CGuard Prime carotid stent system in ...

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

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