
Asclepion-Meditec AG
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LASERSYSTEM BEAUTYSTAR 532 is an FDA 510(k)-cleared medical device (K021975) manufactured by Asclepion-Meditec AG. 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 12, 2002. Regulation: 8.