Mednext, Inc.

Mednext, Inc. — FDA 510(k) Submissions

Mednext, Inc. has submitted 7 FDA 510(k) premarket notifications since 1993, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece, Instrument, Surgical, Orthopedic, Ac-powered Motor And Accessory/attachment, Motor, Surgical Instrument, Ac-powered, Motor, Drill, Pneumatic, Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment . Use the specialty filter in the sidebar to narrow results.