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Progeny, Inc.
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PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). is an FDA 510(k)-cleared medical device (K070664) 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 April 25, 2007. Regulation: 8.