FORCETRIAD

FORCETRIAD is an FDA 510(k)-cleared medical device (K102913) manufactured by Covidien, Formerly Valleylab, A Division of Tyco H. 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 May 5, 2011. Regulation: 8.