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Guilin Woodpecker Medical Instrument Co., Ltd.
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LED.L, LED.M, LED.G, LED.B is an FDA 510(k)-cleared medical device (K080025) manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2008. Regulation: 8.