
A.R. Hinkel Co., Inc.
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ELECTRO-BLEND EPILATOR, MODEL UC-3 is an FDA 510(k)-cleared medical device (K904015) manufactured by A.R. Hinkel Co., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 3, 1990. Regulation: 8.