# Inogen, Inc.

- Location (FDA's records): Goleta, CA
- FDA decisions: 5 (2004–2024): 5 510(k) clearances
- Names in FDA's records: Inogen, Inc. (4); Inogen (1)
- Product codes: CAW (4), SDT (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 14 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Respironics, Inc.: 2 (https://510kreport.com/company/respironics)
- Belluscura, LLC: 1 (https://510kreport.com/company/belluscura)
- Airphysio Pty, Ltd.: 1 (https://510kreport.com/company/airphysio)
- Airsep Corp.: 1 (https://510kreport.com/company/airsep)

## Firms that cite its devices most
- Shenzhen Harveymed Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-harveymed-technology)
- Oxus, Inc.: 1 (https://510kreport.com/company/oxus)
- Vbox, Inc.: 1 (https://510kreport.com/company/vbox)
- Nanjing Yinuoji Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/nanjing-yinuoji-medical-technology)
- Invacare Corp.: 1 (https://510kreport.com/company/invacare)
- Jiangsu Jumao X-Care Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/jiangsu-jumao-x-care-medical-equipment)
- Shenzhen Homed Medical Device Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-homed-medical-device)
- Caire, Inc.: 1 (https://510kreport.com/company/caire)

## Its most-cited devices
- K230052: Inogen Rove 6 (2023), cited by 8
- K032818: Inogen One Oxygen Concentrator (2004), cited by 4
- K222086: Inogen Rove 4 Portable Oxygen Concentrator (2022), cited by 2

## Recent decisions
- K241091: SIMEOX 200 Airway Clearance Device (Dec 23, 2024)
- K230052: Inogen Rove 6 (Jun 30, 2023)
- K222086: Inogen Rove 4 Portable Oxygen Concentrator (Dec 9, 2022)
- K132489: Inogen at Home Oxygen Concentrator (Aka Inogen at Home) (Jun 20, 2014)
- K032818: Inogen One Oxygen Concentrator (May 13, 2004)

Source page: https://510kreport.com/company/inogen