Tactile Systems Technology, Inc. (Tactile Medical) recently announced that Nimbl, its next-generation pneumatic compression ...

The launch of the Get Out the Clot campaign (GetOutTheClot.com) was announced in advance of World Thrombosis Day (WorldThrombos ...

IceCure Medical Ltd. announced new data from the ICE3 trial and five additional studies of the company’s ProSense cryoabla ...

InterVene, Inc., a clinical-stage medical device company that is developing interventional solutions for chronic venous ...

InspireMD, Inc., developer of the CGuard embolic prevention stent system for the prevention of stroke, announced that the FDA ...

Cook Medical announced that it created a custom-made device for the frozen elephant trunk (FET) aortic procedure. The comp ...

Surmodics, Inc. announced it has received FDA 510(k) clearance for its Pounce XL thrombectomy system. The company expects to ...

During the 1980s and early 1990s, the arteriovenous graft was the most common hemodialysis vascular access placed by surgeons in the United States due to favorable reimbursement rates, high technical ...

Canada-based Arrayus Technologies Inc. recently announced that its MRI-guided focused ultrasound system has been granted approva ...

Michael Lieb, DO Vascular Surgeon Virtua Surgical Group Hainesport, New Jersey Disclosures: Consultant to Cagent Vascular.

Deepika Kalisetti, MD Community Health Systems Scranton, Pennsylvania Disclosures: Consultant to Cagent Vascular. CASE STUDY ...

Investigators share case-based perspectives and trial experiences with the Serranator PTA Serration Balloon Catheter, now FDA-cleared for use below the knee. Chronic limb-threatening ischemia (CLTI) ...