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

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

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

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

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 ...

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

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 ...

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 ...