Ethicon Endo-Surgery, Inc.
Ethicon Endo-Surgery, Inc. — FDA 510(k) Submissions
Ethicon Endo-Surgery, Inc. has submitted 112 FDA 510(k) premarket notifications since 1992, of which 112 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Staple, Implantable, Instrument, Ultrasonic Surgical, Endoscopic Tissue Approximation Device, Electrosurgical, Cutting & Coagulation & Accessories . Use the specialty filter in the sidebar to narrow results.
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