DIODENT DENTAL LASER SYSTEM

DIODENT DENTAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K013216) manufactured by Continuum Electro-Optics, 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 February 26, 2002. Regulation: 8.