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Merz Dental GmbH
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MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETH is an FDA 510(k)-cleared medical device (K120404) manufactured by Merz Dental GmbH. 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 20, 2012. Regulation: 8.