
Sunrise Technologies, Inc.
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ADL 400 ND;YAG LASER SYSTEM FOR INTRORAL SOFT TIS. is an FDA 510(k)-cleared medical device (K920106) manufactured by Sunrise Technologies, 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 12, 1992. Regulation: 8.