Soterix Medical, Inc.

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

Soterix Medical, Inc. has submitted 6 FDA 510(k) premarket notifications since 2017, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Electrical, Evoked Response, Device, Iontophoresis, Other Uses, Neurological Stereotaxic Instrument, Stimulator, Nerve, Electrical, Transcutaneous, For Migraine, Transcranial Magnetic Stimulator . Use the specialty filter in the sidebar to narrow results.