Medical Instrument Development Laboratories, Inc.

Medical Instrument Development Laboratories, Inc. — FDA 510(k) Submissions

Medical Instrument Development Laboratories, Inc. has submitted 22 FDA 510(k) premarket notifications since 1982, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Vitreous Aspiration And Cutting, Ac-powered, Unit, Phacofragmentation, Cannula, Ophthalmic, Plug, Scleral, Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment . Use the specialty filter in the sidebar to narrow results.