Endiscope, Endiscope Cervical

Endiscope, Endiscope Cervical is an FDA 510(k)-cleared medical device (K180766) manufactured by Elliquence, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 10, 2018. Regulation: 8.