LightLas Pattern Scanning System - TruScan Pro

LightLas Pattern Scanning System - TruScan Pro is an FDA 510(k)-cleared medical device (K190448) manufactured by Light-Med(Usa), Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 23, 2019. Regulation: 8.