
R-Group Intl.
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ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II. is an FDA 510(k)-cleared medical device (K952470) manufactured by R-Group Intl.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 27, 1995. Regulation: 8.