
Theralight, Inc.
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VERSACLEAR SKIN THERAPY SYSTEM, MODEL 100 is an FDA 510(k)-cleared medical device (K051259) manufactured by Theralight, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 2005. Regulation: 8.