
Omnilight, Inc.
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OMNILIGHT VL-2004, PL-2004, DL-2004, AND WL-2004 is an FDA 510(k)-cleared medical device (K040664) manufactured by Omnilight, Inc.. 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 May 27, 2004. Regulation: 8.