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SW SAFETY SOLUTIONS INC.

US

Last updated May 27, 2026

What SW SAFETY SOLUTIONS INC. makes

SW Safety Solutions Inc. manufactures single-use examination and treatment gloves made from nitrile, polychloroprene, and Hevea latex, all in non-powdered and non-antimicrobial formulations. These gloves are designed for medical, dental, and laboratory use to provide barrier protection during procedures.

The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 SW Safety Solutions Inc. manufacture?

SW Safety Solutions Inc. specializes in single-use examination and treatment gloves. Their products include nitrile, polychloroprene, and Hevea latex gloves, all formulated as non-powdered and non-antimicrobial. These gloves are intended for medical, dental, and laboratory use to create a barrier during procedures.

Where is SW Safety Solutions Inc. based?

SW Safety Solutions Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory context and manufacturing operations.

How are SW Safety Solutions Inc.’s devices classified under FDA regulations?

SW Safety Solutions Inc.’s gloves are classified as Class I medical devices by the FDA. This classification applies to low-risk devices like single-use gloves, which typically require less stringent regulatory oversight compared to higher-risk categories.

Are SW Safety Solutions Inc.’s devices listed in any regulatory databases?

Yes, SW Safety Solutions Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This listing helps ensure traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify product details.

Why are SW Safety Solutions Inc.’s gloves designed without powder or antimicrobials?

The company’s non-powdered and non-antimicrobial gloves are formulated to minimize potential risks such as allergic reactions or contamination. Powder-free gloves reduce the risk of powder-related sensitivities, while non-antimicrobial formulations avoid introducing additional chemicals that could interact with patients or procedures.

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
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DUNS Number
038152115

Catalogue (135)

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DeviceModel / ReferenceRegistriesClassStatus
Sw N091305
FDA UDI
Class IActive
Sw N301342
FDA UDI
Class IActive
Sw N706312
FDA UDI
Class IActive
Sw N027402
FDA UDI
Class IActive
Sw N106551
FDA UDI
Class IActive
Sw N189476
FDA UDI
Class IActive
Sw N901754
FDA UDI
Class IActive
Sw N017751
FDA UDI
Class IActive
Sw N017752
FDA UDI
Class IActive
Sw K071406
FDA UDI
Class IUnknown
Sw K000403
FDA UDI
Class IActive
Sw N017755
FDA UDI
Class IActive
Sw N301341
FDA UDI
Class IActive
Sw N706313
FDA UDI
Class IActive
Sw N260506
FDA UDI
Class IActive
Sw N706315
FDA UDI
Class IActive
Sw N301343
FDA UDI
Class IActive
Sw N127363
FDA UDI
Class IActive
Sw N807717
FDA UDI
Class IActive
Sw N189475
FDA UDI
Class IActive
Sw K071402
FDA UDI
Class IActive
Sw L009203
FDA UDI
Class IActive
Sw K000405
FDA UDI
Class IActive
Sw N129402
FDA UDI
Class IActive
Sw N189473
FDA UDI
Class IActive
Sw N716882
FDA UDI
Class IActive
Sw N127364
FDA UDI
Class IActive
Sw N260884
FDA UDI
Class IActive
Sw N260887
FDA UDI
Class IActive
Sw N991753
FDA UDI
Class IActive
Sw N127362
FDA UDI
Class IActive
Sw N017754
FDA UDI
Class IActive
Sw N106556
FDA UDI
Class IActive
Sw K071405
FDA UDI
Class IActive
Sw N260501
FDA UDI
Class IActive

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