Glidewell 3DP Denture Base Resin

Glidewell 3DP Denture Base Resin is an FDA 510(k)-cleared medical device (K213765) manufactured by Prismatik Dentalcraft, 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 June 21, 2022. Regulation: 8.