Tenax Laser Resistant Endotracheal Tube

Tenax Laser Resistant Endotracheal Tube is an FDA 510(k)-cleared medical device (K200761) manufactured by Bryan Medical, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 2020. Regulation: 8.