Phasor Health, LLC

Phasor Health, LLC — FDA 510(k) Submissions

Phasor Health, LLC has submitted 5 FDA 510(k) premarket notifications since 2025, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Shunt, Central Nervous System And Components, Neurological Stereotaxic Instrument, Drills, Burrs, Trephines & Accessories (simple, Powered), Drills, Burrs, Trephines & Accessories (manual) . Use the specialty filter in the sidebar to narrow results.