LaserCap Family of Lasers 300, 224, 120 & 80

LaserCap Family of Lasers 300, 224, 120 & 80 is an FDA 510(k)-cleared medical device (K203826) manufactured by Transdermal Cap, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 2021. Regulation: 8.