NuFACE FIX Skin Toning Device

NuFACE FIX Skin Toning Device is an FDA 510(k)-cleared medical device (K182424) manufactured by Carol Cole Company Dba Nuface. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 2018. Regulation: 8.