
Artech Corp.
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HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL is an FDA 510(k)-cleared medical device (K894160) manufactured by Artech Corp.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 27, 1989. Regulation: 8.