
Discus Dental, Inc.
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MEGA BITE REGISTRATION - DENTAL BITE REGISTRATION MATERIAL is an FDA 510(k)-cleared medical device (K030776) manufactured by Discus Dental, 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 May 8, 2003. Regulation: 8.