BONE PLUS BCP EAGLE EYE

BONE PLUS BCP EAGLE EYE is an FDA 510(k)-cleared medical device (K122240) manufactured by Megagen Implant Co., Ltd.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 20, 2012. Regulation: 8.