
Dynatronics Corp.
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DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE is an FDA 510(k)-cleared medical device (K113250) 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 February 8, 2012. Regulation: 8.