FILTEK BULK FILL POSTERIOR RESTROATIVE

FILTEK BULK FILL POSTERIOR RESTROATIVE is an FDA 510(k)-cleared medical device (K141081) manufactured by 3M Espe Dental Products. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 2014. Regulation: 8.