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Progeny, Inc.
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PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015 is an FDA 510(k)-cleared medical device (K043092) manufactured by Progeny, 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 December 12, 2004. Regulation: 8.