Karl Storz Endoscopy

Karl Storz Endoscopy — FDA 510(k) Submissions

Karl Storz Endoscopy has submitted 35 FDA 510(k) premarket notifications since 1995, of which 35 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Arthroscope, Hysteroscope (and Accessories), Endoscope, Neurological, Screw, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.