LightForce LTS Model 1000, 1500, 2500, and 4000

LightForce LTS Model 1000, 1500, 2500, and 4000 is an FDA 510(k)-cleared medical device (K173067) manufactured by Litecure, LLC. 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 February 21, 2018. Regulation: 8.