Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 is an FDA 510(k)-cleared medical device (K160285) manufactured by Capillus, LLC. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 24, 2016. Regulation: 8.