DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980

DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980 is an FDA 510(k)-cleared medical device (K063384) manufactured by Hoya Conbio, 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 15, 2007. Regulation: 8.