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Honeywell 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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LinkedIn
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Facebook
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Email
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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
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Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Honeywell Performance Exam Glove 4580601–M
FDA UDI
Class IActive
Honeywell Performance Exam Glove 4580601-L
FDA UDI
Class IActive
Surgical Mask 559250P
FDA UDI
Class IIActive

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