Avenu Medical, Inc.

Avenu Medical, Inc. — FDA 510(k) Submissions

Avenu Medical, Inc. has submitted 3 FDA 510(k) premarket notifications since 2018, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis Access . Use the specialty filter in the sidebar to narrow results.