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Caldera Medical, Inc.
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VERTESSA LITE 10 X20CM, VERTESSA LITE 11 X 30CM, VERTESSA LITE Y-MESH is an FDA 510(k)-cleared medical device (K123028) manufactured by Caldera Medical, 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 April 24, 2013. Regulation: 8.