BOND-IT DUAL CURE ACTIVATOR

BOND-IT DUAL CURE ACTIVATOR is an FDA 510(k)-cleared medical device (K953859) manufactured by Jeneric/Pentron, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 6, 1995. Regulation: 8.