
J. Morita USA, Inc.
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ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A is an FDA 510(k)-cleared medical device (K120377) manufactured by J. Morita USA, 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 July 24, 2012. Regulation: 8.