Nexus Universal, Nexus Universal Chroma

Nexus Universal, Nexus Universal Chroma is an FDA 510(k)-cleared medical device (K151332) manufactured by Sybron Dental Specialties. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 16, 2015. Regulation: 8.