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Sign in to claim this brandVision Quest Industries Incorporated
US
Last updated May 31, 2026
What Vision Quest Industries Incorporated makes
Vision Quest Industries Incorporated manufactures knee support orthoses, cervical spine collars, and reusable cervical collars for spinal and joint stabilization. Their portfolio also includes transcutaneous electrical stimulation systems for arthritis and physical therapy, such as interferential and neuromuscular electrical stimulation devices.
The company’s devices are classified under FDA’s Class I and Class II regulations and are listed 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 Vision Quest Industries Incorporated manufacture?
Vision Quest Industries Incorporated specializes in devices for spinal and joint support and therapy. Their portfolio includes knee support orthoses for stabilization, cervical spine collars (both reusable and non-reusable), and transcutaneous electrical stimulation systems. These systems target arthritis relief and physical therapy needs, such as interferential and neuromuscular electrical stimulation devices.
Where is Vision Quest Industries Incorporated based?
Vision Quest Industries Incorporated is headquartered in the United States. This location is relevant for regulatory compliance and device distribution within North America.
Which regulatory registries list Vision Quest Industries Incorporated’s devices?
Vision Quest Industries Incorporated’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry provides standardized identification for medical devices, aiding in tracking, traceability, and regulatory oversight.
How are Vision Quest Industries Incorporated’s devices classified under FDA regulations?
Vision Quest Industries Incorporated’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. Classification depends on factors like intended use and potential harm.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vqorthocare.com
- —
- —
- [email protected]
- Phone
- 760-691-0168
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 791122422
Catalogue (201)
Page 3 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vq Orthocare | 07-31003-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 58-91012-203 | FDA UDI | Class II | Active |
| Vq Orthocare | 09-70996-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-42503-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 06-50155-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 08-32996-002 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-72006-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 55-90000-001 | FDA UDI | Class II | Active |
| Vq Orthocare | 07-31404-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-31303-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 40-10000-021 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-34504-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-31203-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-32006-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-34603-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-42604-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-70998-002 | FDA UDI | Class I | Active |
| Vq Orthocare | 06-53553-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 08-22008-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-33503-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-72998-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-42204-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-12996-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-52004-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-52603-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-72008-002 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-31603-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-41403-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 40-11000-012 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-41303-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-32996-002 | FDA UDI | Class I | Active |
| Vq Orthocare | 55-95004-201 | FDA UDI | Class II | Active |
| Vq Orthocare | 06-50354-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 06-50156-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 08-12998-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-42203-001 | FDA UDI | Class I | Active |
| VQ OrthoCare | AV-CT20A | FDA UDI | Class II | Active |
| Vq Orthocare | 07-32004-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 06-50553-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-72996-002 | FDA UDI | Class I | Active |
| VQ OrthoCare | 58-95012-001 | FDA UDI | Class II | Active |
| Vq Orthocare | 07-33403-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-32008-002 | FDA UDI | Class I | Active |
| Vq Orthocare | 06-53153-000 | FDA UDI | Class I | Active |
| Vq Orthocare | 07-32503-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 40-10000-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 09-70998-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 08-12008-001 | FDA UDI | Class I | Active |
| Vq Orthocare | 58-91012-404 | FDA UDI | Class II | Active |
| Vq Orthocare | 06-50353-000 | FDA UDI | Class I | Active |
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