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Sign in to claim this brandSTRONGBACK MOBILITY USA, LLC
US
Last updated May 24, 2026
What STRONGBACK MOBILITY USA, LLC makes
The company manufactures collapsible attendant/occupant-driven wheelchairs with rear-wheel operation, foldable non-powered handgrip walkers for disability assistance, and bariatric push-rim manual wheelchairs. These devices are designed for mobility support in various settings, including home and clinical environments.
All listed devices fall under Class I regulatory classification in the US and are registered in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Strongback Mobility USA, LLC manufacture?
Strongback Mobility USA, LLC specializes in mobility assistance devices, including collapsible wheelchairs operated by attendants or occupants via rear wheels, foldable non-powered walkers with handgrips for disability support, and bariatric push-rim manual wheelchairs. These products are designed to provide flexible and durable mobility solutions for users in home or clinical settings.
Where is Strongback Mobility USA, LLC based?
The company is headquartered in the United States. This location ensures compliance with US regulatory standards, including those governing medical device manufacturing and distribution.
Which regulatory registries list Strongback Mobility USA, LLC’s devices?
Strongback Mobility USA, LLC’s devices are registered in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the US market, ensuring transparency and traceability for healthcare providers and regulators.
How are Strongback Mobility USA, LLC’s devices classified under US regulations?
All of Strongback Mobility USA, LLC’s listed devices fall under Class I regulatory classification in the US. This classification applies to low-risk devices that pose minimal potential harm to users, such as mobility aids like wheelchairs and walkers, which typically require less stringent premarket review.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- strongbackmobility.com
- —
- —
- [email protected]
- Phone
- +1 757 349 7790
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 040262426
Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Strongback | 1007+AB/023 | FDA UDI | Class I | Active |
| Strongback | 1003+AB/020 | FDA UDI | Class I | Active |
| Strongback | 1002/016 | FDA UDI | Class I | Active |
| Strongback | 1010+AB/024 | FDA UDI | Class I | Active |
| Strongback | 1003/018 | FDA UDI | Class I | Active |
| Strongback | 1019/008 | FDA UDI | Class I | Active |
| Strongback | 1017/001 | FDA UDI | Class I | Active |
| Strongback | SEATA Rollator | FDA UDI | Class I | Active |
| Strongback | 1007/002 | FDA UDI | Class I | Active |
| Strongback | 1012+AB/026 | FDA UDI | Class I | Active |
| Strongback | 1036+AB/053 | FDA UDI | Class I | Active |
| Strongback | 1016+AB/036 | FDA UDI | Class I | Active |
| Strongback | 1017+AB/029 | FDA UDI | Class I | Active |
| Strongback | 1010/003 | FDA UDI | Class I | Active |
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