DIODENT II DENTAL LASER SYSTEM

DIODENT II DENTAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K050274) manufactured by Hoya Photonics, 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 April 28, 2005. Regulation: 8.