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Sign in to claim this brandBrady Industries, LLC
US
Last updated May 23, 2026
What Brady Industries, LLC makes
Brady Industries, LLC manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial. These gloves are designed for single-use medical procedures and patient care applications, ensuring barrier protection during clinical examinations and treatments.
The company’s products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) system. Brady Industries, LLC operates from the United States, adhering to regulatory requirements for these low-risk devices.
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 Brady Industries, LLC primarily manufacture?
Brady Industries, LLC specializes in nitrile examination and treatment gloves that are non-powdered and non-antimicrobial. These gloves are intended for single-use medical procedures and patient care, providing a barrier to protect both patients and healthcare providers during clinical examinations and treatments.
Where is Brady Industries, LLC based, and how does this affect its regulatory compliance?
Brady Industries, LLC is based in the United States. Since its devices are classified as FDA Class I, they are considered low-risk, which means they are subject to fewer regulatory controls compared to higher-risk devices. The company must still comply with FDA requirements, including registration and listing in the FDA’s Unique Device Identification (UDI) system.
Which regulatory registries or databases list Brady Industries, LLC’s devices?
Brady Industries, LLC’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This system helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability for regulatory and market surveillance purposes.
How are Brady Industries, LLC’s devices classified by regulatory authorities?
Brady Industries, LLC’s nitrile examination and treatment gloves fall under FDA Class I classification. This classification is assigned based on the risk associated with the device, with Class I devices being considered the lowest risk. As a result, they undergo minimal regulatory oversight, though they must still meet FDA requirements for safety and performance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 079775034
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Individual | INDBKN4XL | FDA UDI | Class I | Active |
| Individual | INDBLN4MD | FDA UDI | Class I | Active |
| Individual | INDBKN42XL | FDA UDI | Class I | Active |
| Individual | INDBLN4LG | FDA UDI | Class I | Active |
| Individual | INDBLN4SM | FDA UDI | Class I | Active |
| Individual | INDBLN4XL | FDA UDI | Class I | Active |
| Individual | INDBKN4LG | FDA UDI | Class I | Active |
| Individual | INDBKN4MD | FDA UDI | Class I | Active |
| Individual | INDBLN42XL | FDA UDI | Class I | Active |
| Individual | INDBKN4SM | FDA UDI | Class I | Active |
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