Medtronic Completes Acquisition of Scientia Vascular

June 12, 2026—Medtronic announced it has completed its acquisition of Scientia Vascular, a privately held developer of access products for the treatment of complex neurovascular conditions.

Spectrum Vascular Acquires Piccolo Medical

June 12, 2026—Spectrum Vascular announced the acquisition of Piccolo Medical, a developer of catheter guidance products.

WaveClear Licenses Resolution Thrombectomy Technology to Two Chinese Companies

June 12, 2026—WaveClear Vascular, developer of the Resolution cavitation system, announced that it has entered into licensing agreements with two Chinese medical device companies for Resolution, a 6-F catheter-based thrombectomy platform for the treatment of peripheral vascular disease.

Penumbra’s Thunderbolt CAVT Platform Cleared by FDA for Stroke Treatment

June 11, 2026—Penumbra, Inc. announced it has received FDA clearance for the Thunderbolt computer-assisted vacuum thrombectomy (CAVT) platform for the treatment of acute ischemic stroke.

Ventiv Scientific’s V-Pulse Mechanical Thrombectomy System Used in FIH Procedures 

June 11, 2026—Ventiv Scientific announced the completion of the first-in-human (FIH) clinical procedures with its V-Pulse mechanical thrombectomy system.

Complete Adherence to Guideline-Directed Care in PAD Shows Decreased MALE at 2 Years

June 10, 2026—The Society for Vascular Surgery (SVS) announced that new study data show that patients with peripheral artery disease who adhere to preoperative guideline-directed care (GDC) are more likely to remain free from major adverse limb events (MALE) for up to 2 years after intervention.

FDA Approves CyndRx’s AbsorbaSeal Vascular Closure Device

June 9, 2026—CyndRx, LLC, announced FDA approval of its AbsorbaSeal vascular closure device.

Gore Viabahn Fortegra Venous Stent Receives CE Mark Approval Under EU MDR

June 9, 2026—Gore & Associates announced CE Mark approval for its Viabahn Fortegra venous stent, indicated for use in the treatment of symptomatic inferior vena cava (IVC) and iliofemoral venous outflow obstruction. The approval is granted under the European Union Medical Device Regulation.