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Teleflex Medical
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FORCE FIBER POLYETHYLENE NONABSORBABLE SUTURE is an FDA 510(k)-cleared medical device (K063778) 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 February 8, 2007. Regulation: 8.