
Smith & Nephew Richards, Inc.
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ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY is an FDA 510(k)-cleared medical device (K935235) manufactured by Smith & Nephew Richards, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 1995. Regulation: 8.