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Sign in to claim this brandCENTRAL ASSOCIATION FOR THE BLIND, INC.
US
Last updated May 23, 2026
What CENTRAL ASSOCIATION FOR THE BLIND, INC. makes
The company produces single-use examination and treatment gloves made from nitrile, hevea latex, and vinyl, all in non-powdered and non-antimicrobial formulations. It also manufactures a dural mater sealant, a surgical material used to close or reinforce the protective membrane surrounding the brain and spinal cord.
All listed devices fall under Class I regulation in the US, with each product authorised through the FDA’s Unique Device Identification (UDI) system. 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 Central Association for the Blind, Inc. manufacture?
Central Association for the Blind, Inc. primarily manufactures single-use medical gloves and a dural mater sealant. The gloves include nitrile, hevea latex, and vinyl formulations, all in non-powdered and non-antimicrobial versions. The dural mater sealant is used to reinforce or close the protective membrane around the brain and spinal cord.
Where is Central Association for the Blind, Inc. based?
The company is based in the United States. This location is relevant for regulatory compliance, as it aligns with the FDA’s jurisdiction over medical devices authorised in the US.
How are Central Association for the Blind, Inc.’s devices classified under US regulations?
All of the company’s devices fall under Class I regulation in the US. This classification applies to low-risk medical products, where the FDA’s oversight is generally limited to ensuring proper labelling and manufacturing controls. Each device is authorised through the FDA’s Unique Device Identification (UDI) system, which helps track and trace products in the supply chain.
Which regulatory registries or databases list Central Association for the Blind, Inc.’s devices?
The company’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures transparency and traceability of medical products authorised for use in the US, allowing healthcare providers and regulators to verify device details.
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
- 099903148
Catalogue (37)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Better Touch | 807.2 | FDA UDI | Class I | Active |
| Better Touch | 880.4 | FDA UDI | Class I | Active |
| Better Touch | 804.2 | FDA UDI | Class I | Active |
| Better Touch | 825.4 | FDA UDI | Class I | Active |
| Better Touch | 804.5 | FDA UDI | Class I | Active |
| Better Touch | 880.2 | FDA UDI | Class I | Active |
| Better Touch | 807.5HHC | FDA UDI | Class I | Active |
| Better Touch | 802.3 | FDA UDI | Class I | Active |
| Better Touch | 880.1 | FDA UDI | Class I | Active |
| Better Touch | 809.1 | FDA UDI | Class I | Active |
| Better Touch | 807.3HHC | FDA UDI | Class I | Active |
| Better Touch | 807.4HHC | FDA UDI | Class I | Active |
| Better Touch | 825.6 | FDA UDI | Class I | Active |
| Better Touch | 804.4 | FDA UDI | Class I | Active |
| Better Touch | 807.6 | FDA UDI | Class I | Active |
| Better Touch | 809.4 | FDA UDI | Class I | Active |
| Better Touch | 880.6 | FDA UDI | Class I | Active |
| Better Touch | 802.1 | FDA UDI | Class I | Active |
| Better Touch | 802.5 | FDA UDI | Class I | Active |
| Better Touch | 809.2 | FDA UDI | Class I | Active |
| Better Touch | 807.4 | FDA UDI | Class I | Active |
| Better Touch | 807.5 | FDA UDI | Class I | Active |
| Better Touch | 802.4 | FDA UDI | Class I | Active |
| Better Touch | 807.1 | FDA UDI | Class I | Active |
| Better Touch | 809.5 | FDA UDI | Class I | Active |
| Better Touch | 809.3 | FDA UDI | Class I | Active |
| Better Touch | 809.6 | FDA UDI | Class I | Active |
| Better Touch | 807.2HHC | FDA UDI | Class I | Active |
| Better Touch | 880.5 | FDA UDI | Class I | Active |
| Better Touch | 802.2 | FDA UDI | Class I | Active |
| Better Touch | 807.3 | FDA UDI | Class I | Active |
| Better Touch | 825.5 | FDA UDI | Class I | Active |
| Better Touch | 825.2 | FDA UDI | Class I | Active |
| Better Touch | 880.3 | FDA UDI | Class I | Active |
| Better Touch | 825.3 | FDA UDI | Class I | Active |
| Better Touch | 809.7 | FDA UDI | Class I | Active |
| Better Touch | 804.3 | FDA UDI | Class I | Active |
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