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Tei Biosciences, Inc.
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TISSUEMEND SOFT TISSUE REPAIR MATRIX is an FDA 510(k)-cleared medical device (K060989) manufactured by Tei Biosciences, 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 May 14, 2006. Regulation: 8.