
Cox-Uphuff Intl.
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CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER is an FDA 510(k)-cleared medical device (K874276) manufactured by Cox-Uphuff Intl.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 1, 1987. Regulation: 8.