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G & H Wire Co.
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ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREW is an FDA 510(k)-cleared medical device (K081393) manufactured by G & H Wire Co.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 20, 2008. Regulation: 8.