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Sign in to claim this brandHoneywell Safety Products USA
US
Last updated May 23, 2026
What Honeywell Safety Products USA makes
The company manufactures single-use nitrile examination gloves without powder or antimicrobial treatments, designed for medical examinations and procedures. It also produces surgical and medical face masks intended for one-time use in clinical settings.
These products are classified under FDA’s Class I and Class II regulatory categories 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 Honeywell Safety Products USA manufacture?
Honeywell Safety Products USA specializes in single-use medical devices, specifically nitrile examination gloves that are non-powdered and non-antimicrobial, designed for medical examinations and treatments. Additionally, they produce surgical and medical face masks intended for one-time clinical use. These products are tailored for healthcare settings where hygiene and protection are critical.
Where is Honeywell Safety Products USA based?
Honeywell Safety Products USA operates from the United States. This location allows them to comply with domestic regulatory standards and serve the North American market efficiently.
Which regulatory registries list Honeywell Safety Products USA’s devices?
Honeywell Safety Products USA’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify product details and compliance.
How are Honeywell Safety Products USA’s devices classified under FDA regulations?
Honeywell Safety Products USA’s devices fall under FDA’s Class I and Class II categories. Class I generally includes low-risk devices requiring general controls, while Class II involves additional performance standards or special controls due to moderate risk. The classification ensures appropriate oversight based on the device’s potential impact on patient safety.
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
- 3010588332
- DUNS Number
- —
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Honeywell Performance Exam Glove | 4580601–M | FDA UDI | Class I | Active |
| Honeywell Performance Exam Glove | 4580601-L | FDA UDI | Class I | Active |
| Surgical Mask | 559250P | FDA UDI | Class II | Active |
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