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Sign in to claim this brandSOLVAY SPECIALTY POLYMERS USA, L.L.C.
US
Last updated May 25, 2026
What SOLVAY SPECIALTY POLYMERS USA, L.L.C. makes
Solvay Specialty Polymers USA, LLC manufactures thermoplastic materials specifically designed for dental appliance fabrication, including milling discs used in dental milling processes. These materials are engineered to support precision cutting and shaping in dental laboratories.
The company’s products fall under FDA Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Solvay Specialty Polymers USA, LLC primarily manufacture?
Solvay Specialty Polymers USA, LLC specializes in thermoplastic materials used for dental appliance fabrication. Their most common product category is dental appliance fabrication material, specifically milling discs designed for precision cutting and shaping in dental laboratories. These materials are tailored for use in dental milling processes to ensure accuracy and efficiency.
Where is Solvay Specialty Polymers USA, LLC based?
The company is headquartered in the United States. This location allows them to focus on developing and distributing thermoplastic materials tailored to the needs of dental professionals and laboratories within the region.
Which regulatory registries or databases list Solvay Specialty Polymers USA, LLC’s devices?
Solvay Specialty Polymers USA, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify product details.
How are Solvay Specialty Polymers USA, LLC’s devices classified by regulatory authorities?
The company’s devices fall under FDA Class II classification. This classification is typically assigned to devices that have a moderate level of risk and require special controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
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
- 094731705
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dentivera Milling Disc | A008 | FDA UDI | Class II | Active |
| Dentivera Milling Disc | A001 | FDA UDI | Class II | Active |
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