
Acell, Inc.
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Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix Extend is an FDA 510(k)-cleared medical device (K170763) manufactured by Acell, 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 June 7, 2017. Regulation: 8.