XPEED ANYRIDGE INTERNAL IMPLANT SYSTEM

XPEED ANYRIDGE INTERNAL IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K123870) 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 March 26, 2013. Regulation: 8.