ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT is an FDA 510(k)-cleared medical device (K082071) manufactured by Adpharma, 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 October 1, 2008. Regulation: 8.