
Heraeus Lasersonics, Inc.
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MDLS 4000/4900/6000/8000/8900/LUXUS 60/100 ND:YAG is an FDA 510(k)-cleared medical device (K903444) manufactured by Heraeus Lasersonics, 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 October 10, 1990. Regulation: 8.