Atlantis Abutment for MIS Implant

Atlantis Abutment for MIS Implant is an FDA 510(k)-cleared medical device (K172225) manufactured by Dentsply Sirona. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 29, 2017. Regulation: 8.