Inogen, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241091SIMEOX 200 Airway Clearance DeviceDecember 23, 2024
K230052Inogen Rove 6June 30, 2023
K222086Inogen Rove 4 Portable Oxygen ConcentratorDecember 9, 2022
K132489INOGEN AT HOME OXYGEN CONCENTRATOR (AKA INOGEN AT HOME)June 20, 2014
K032818INOGEN ONE OXYGEN CONCENTRATORMay 13, 2004