Calyxo, Inc.

Calyxo, Inc. — FDA 510(k) Submissions

Calyxo, Inc. has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ureteroscope And Accessories, Flexible/rigid, Endoscopic Access Overtube, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.