BONALIVE GRANULES AND BONALIVE PLATES

BONALIVE GRANULES AND BONALIVE PLATES is an FDA 510(k)-cleared medical device (K070055) manufactured by Vivoxid , 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 June 24, 2007. Regulation: 8.