Inogen, Inc. - FDA 510(k) Cleared Devices

Inogen, Inc. has 4 FDA 510(k) cleared medical devices. Based in Goleta, US.

Latest FDA clearance: Dec 2024. Active since 2004. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Inogen, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Nilo Medical Consulting Group as regulatory consultant.