Inogen, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
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.
FDA 510(k) cleared devices by Inogen, Inc.
4 devices