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Inogen At Home Stationary Concentrator
FDA UDIClass II (US FDA UDI)
by Inogen, Inc.
Identity
- Trade Name
- Inogen At Home Stationary Concentrator FDA UDI
- Generic Name
- Stationary oxygen concentrator FDA UDI
- Device Name
- Inogen At Home Stationary Concentrator, NCE (10-05345-XX-XX) FDA UDI
- Model / Reference
- NCE FDA UDI
- Description
- Inogen At Home Stationary Concentrator, NCE (10-05345-XX-XX) FDA UDI
Identifiers
- Catalog Number
- GS-100 FDA UDI
- Primary DI / UDI-DI
- 00817131020131 FDA UDI
- 510(k) Number
- K132489 FDA UDI
- FDA Product Code
- CAW FDA UDI
- GMDN Term
- Stationary oxygen concentrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5440 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Stationary oxygen concentrator
Inogen At Home Stationary Concentrator by Inogen, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Stationary oxygen concentrator.
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- NewLife Intensity — Airsep Corp. · Class II
- DeVilbiss — DeVilbiss Healthcare LLC. · Class II
- Oxygen Concentrator — Proactive Medical Products · Class II
Cleared under the same submission
K132489 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Inogen, Inc.
Sources (1)
- FDA UDI 554f244e-5d2e-4067-a60b-4ecb98f915c1 37 fields · synced May 31, 2026