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Teleflex Medical
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FORCE FIBER BLUE CO-BRAIDED POLYETHYLENE NONABSORBABLE SURGICAL SUTURE is an FDA 510(k)-cleared medical device (K040472) manufactured by Teleflex Medical. 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 March 14, 2004. Regulation: 8.