
Jeneric/Pentron, Inc.
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CEMENT IT! UNIVERSAL C&B is an FDA 510(k)-cleared medical device (K000173) 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 February 28, 2000. Regulation: 8.