Picasso Pro Diode Laser (002-00460)

Picasso Pro Diode Laser (002-00460) is an FDA 510(k)-cleared medical device (K254197) manufactured by CAO Group, Inc.. 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 March 10, 2026. Regulation: 8.