
Aventix Medical, Inc.
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AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001) is an FDA 510(k)-cleared medical device (K260255) manufactured by Aventix Medical, 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 March 26, 2026. Regulation: 8.