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Sign in to claim this brandValley Contax, Inc.
US
Last updated May 30, 2026
What Valley Contax, Inc. makes
Valley Contax, Inc. manufactures rigid-gas-permeable contact lenses designed for daily wear, including single-vision, multifocal, and scleral variants. Their portfolio includes custom-fitted lenses such as the Custom Stable series, as well as specific materials like roflufocon D, tisilfocon A, and enflufocon A for different vision correction needs.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) and Unique Device Identification (UDI) pathways. The company’s products are listed in the FDA’s regulatory databases, and 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 Valley Contax, Inc. manufacture?
Valley Contax, Inc. specialises in rigid-gas-permeable (RGP) corrective contact lenses designed for daily wear. These include single-vision lenses, multifocal lenses like the Valley Contax Goldeneye Aspheric Front Multifocal (AFM), and custom-fitted scleral lenses such as the Custom Stable series. The lenses are made from various materials like roflufocon D, tisilfocon A, and enflufocon A to address different vision correction needs.
Where is Valley Contax, Inc. based?
Valley Contax, Inc. is headquartered in the United States. The company’s location is relevant for regulatory oversight, as its devices are authorised under U.S. regulatory frameworks like the FDA’s 510(k) and UDI systems.
Which regulatory registries or databases list Valley Contax’s devices?
Valley Contax’s devices are listed in the FDA’s regulatory databases, specifically through the 510(k) premarket notification process and the Unique Device Identification (UDI) system. These registries ensure traceability and compliance with U.S. medical device regulations.
How are Valley Contax’s devices classified under FDA regulations?
All of Valley Contax’s listed devices fall under Class II classification by the FDA. This classification applies to products that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as rigid-gas-permeable contact lenses.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 013969530
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Custom Stable | Optimum Exra (roflufocon D) Clear | FDA UDI | Class II | Active |
| Custom Stable | Optimum Exra (roflufocon D) Light Blue | FDA UDI | Class II | Active |
| Custom Stable | Optimum Extreme (roflufocon E) Clear | FDA UDI | Class II | Active |
| Custom Stable | Optimum Extreme (roflufocon E) Light Blue | FDA UDI | Class II | Active |
| Custom Stable Rigid Gas Permeable Scleral Contact Lens | K213880 | FDA 510(k) | Class II | Active |
| Custom Stable(TM) Rigid Gas Permeable Scleral Contact Lens | K170335 | FDA 510(k) | Class II | Active |
| Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax Goldeneye Aspheric Front Multifocal (AFM) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax V Kone (VK) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A) | K202860 | FDA 510(k) | Class II | Active |
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