
Teleflexmedical, Inc.
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FORCE FIBER BLACK CO-BRAID POLYETHYLENE NON-ABSORBABLE SURGICAL SUTURE is an FDA 510(k)-cleared medical device (K070673) manufactured by Teleflexmedical, Inc.. 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 April 1, 2007. Regulation: 8.