
Progeny, Inc.
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VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 is an FDA 510(k)-cleared medical device (K090079) manufactured by Progeny, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 30, 2009. Regulation: 8.