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Amd Lasers, LLC
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PICASSO/ PICASSO LITE/ PICASSO PERIO is an FDA 510(k)-cleared medical device (K102359) manufactured by Amd Lasers, 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 September 15, 2011. Regulation: 8.