
Allmed Systems, Inc.
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REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200 is an FDA 510(k)-cleared medical device (K110941) manufactured by Allmed Systems, 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 February 18, 2013. Regulation: 8.