
STERIS Corporation
Free shipping on orders over $99 · 30-day returns
Avulsion Forceps is an FDA 510(k)-cleared medical device (K183428) manufactured by STERIS Corporation. 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 April 15, 2019. Regulation: 8.