LIPSONIX(R) SYSTEM MODEL 2

LIPSONIX(R) SYSTEM MODEL 2 is an FDA 510(k)-cleared medical device (K112626) manufactured by Medicis Technologies Corporation. 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 October 19, 2011. Regulation: 8.