LISTERINE Sensitivity Defense Mouthrinse

LISTERINE Sensitivity Defense Mouthrinse is an FDA 510(k)-cleared medical device (K143155) manufactured by Johnson & Johnson Healthcare Products, Division of Mcneil-Pp. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 28, 2015. Regulation: 8.