
Fujifilm New Development U.S.A., Inc.
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InterLock Trocar is an FDA 510(k)-cleared medical device (K170084) manufactured by Fujifilm New Development U.S.A., 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 9, 2017. Regulation: 8.