
Miret Surgical, Inc.
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Miret Grasper, Alligator, Miret Grasper, Maryland is an FDA 510(k)-cleared medical device (K160149) manufactured by Miret Surgical, 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 August 29, 2016. Regulation: 8.