Medivis, Inc.

Medivis, Inc. — FDA 510(k) Submissions

Medivis, Inc. has submitted 3 FDA 510(k) premarket notifications since 2019, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Image Processing, Radiological, Neurological Stereotaxic Instrument, Orthopedic Stereotaxic Instrument . Use the specialty filter in the sidebar to narrow results.