EndoTool IV Cloud 1.0

EndoTool IV Cloud 1.0 is an FDA 510(k)-cleared medical device (K260910) manufactured by Glooko, 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 April 30, 2026. Regulation: 8.