Multi-unit Abutments for CONELOG

Multi-unit Abutments for CONELOG is an FDA 510(k)-cleared medical device (K203252) manufactured by BioHorizons Implant Systems, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 2021. Regulation: 8.