Sonomotion, Inc.

Sonomotion, Inc. — FDA 510(k) Submissions

Sonomotion, Inc. has submitted 2 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ultrasonic Urinary Stone Propulsion Device, Lithotriptor, Extracorporeal Shock-wave, Urological . Use the specialty filter in the sidebar to narrow results.