Vein 360, LLC

Vein 360, LLC — FDA 510(k) Submissions

Vein 360, LLC has submitted 4 FDA 510(k) premarket notifications since 2019, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reprocessed Intravascular Ultrasound Catheter, Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed . Use the specialty filter in the sidebar to narrow results.