Hem-o-lok® Ligating Clips

Hem-o-lok® Ligating Clips is an FDA 510(k)-cleared medical device (K232970) manufactured by Teleflex Medical. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2024. Regulation: 8.