Prodeon Medical, Inc.

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

Prodeon Medical, Inc. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Access Overtube, Gastroenterology-urology, Temporarily-placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia . Use the specialty filter in the sidebar to narrow results.