Konig Bell Circumcision Clamp

Konig Bell Circumcision Clamp is an FDA 510(k)-cleared medical device (K251687) manufactured by Medline Industries, LP. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 24, 2026. Regulation: 8.