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Dynatronics Corp.
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DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE is an FDA 510(k)-cleared medical device (K051261) manufactured by Dynatronics Corp.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 2005. Regulation: 8.