Clio Prime and Clio Pedo

Clio Prime and Clio Pedo is an FDA 510(k)-cleared medical device (K202664) manufactured by Sota Precision Optics, Inc. Dba Sota Imaging. 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 5, 2020. Regulation: 8.