ANKYLOS DENTAL IMPLANT SYSTEM

ANKYLOS DENTAL IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K041509) manufactured by Friadent GmbH. 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 25, 2004. Regulation: 8.