Storz Instrument Co.
Storz Instrument Co. — FDA 510(k) Submissions
Storz Instrument Co. has submitted 101 FDA 510(k) premarket notifications since 1976, of which 100 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Unit, Phacofragmentation, Instrument, Vitreous Aspiration And Cutting, Ac-powered, System, Imaging, Pulsed Echo, Ultrasonic, Electrosurgical, Cutting & Coagulation & Accessories, Microscope, Surgical . Use the specialty filter in the sidebar to narrow results.
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