Datex-Ohmeda, Inc. - FDA 510(k) Cleared Devices

Datex-Ohmeda, Inc. has 62 FDA 510(k) cleared anesthesiology devices. Based in Madison, US.

Latest FDA clearance: Aug 2026. Active since 1998.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Datex Ohmeda, Inc. as regulatory consultant.