QuikClot Control+ Hemostatic Device

QuikClot Control+ Hemostatic Device is an FDA 510(k)-cleared medical device (K243553) 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 March 17, 2025. Regulation: 8.