
Zinnanti Surgical Instruments, Inc.
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FORCEPS FOR LAPAROSCOPIC SURGERY GU USE is an FDA 510(k)-cleared medical device (K925959) manufactured by Zinnanti Surgical Instruments, 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 November 11, 1993. Regulation: 8.