Lite-Med, Inc.

Lite-Med, Inc. — FDA 510(k) Submissions

Lite-Med, Inc. has submitted 3 FDA 510(k) premarket notifications since 2011, of which 3 received clearance as substantially equivalent to a predicate device.

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