ABK Biomedical, Inc. announced the completion of patient enrollment in the ROUTE90 pivotal study evaluating the company’ ...

February 24, 2026—iVascular announced the enrollment of the first patient in the FENCO clinical study evaluating the company’s iCover ball ...

Liquet Medical Inc. announced it has received a second FDA 510(k) clearance for a new configuration of its Versus cathete ...

The 2026 AHA/ACC guidelines introduce a five-tier Acute PE Clinical Category system to stratify severity and guide treatment decisions. Mechanical thrombectomy receives a Class 2a recommendation for ...

AngioDynamics, Inc. announced expanded European indications for its NanoKnife system with irreversible electroporation (IRE) ...

Medtronic plc announced that Japan’s Ministry of Health, Labour and Welfare (MHLW) has granted reimbursement approval fo ...

Bayer recently reported that its oral factor XIa inhibitor asundexian reduced the risk of recurrent ischemic stroke in patient ...

Sentante announced that its Sentante stroke system has been accepted into the FDA Total Product Life Cycle Advisory Program ...

Irish medtech company InVera Medical announced the CE Mark approval of its InVera Infusion Device. The device may now be marke ...

Rampart, a Birmingham, Alabama–based medical device company focused on radiation safety in the interventional suite, ann ...