Midmark Extraoral Imaging System (EOIS)

Midmark Extraoral Imaging System (EOIS) is an FDA 510(k)-cleared medical device (K201667) manufactured by Midmark Corporation. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 2020. Regulation: 8.