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LIBERTY GLOVE & SAFETY, LLC

US

Last updated May 23, 2026

What LIBERTY GLOVE & SAFETY, LLC makes

Liberty Glove & Safety, LLC manufactures examination and treatment gloves, including nitrile and hevea-latex varieties that are non-powdered and non-antimicrobial. The company also produces thermal vapour lung treatment system catheters, designed for medical procedures requiring controlled vapor delivery.

All devices are classified as Class I under regulatory frameworks, with relevant products 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 Liberty Glove & Safety, LLC primarily manufacture?

Liberty Glove & Safety, LLC specializes in gloves and catheters used in medical settings. Their most common products are nitrile and hevea-latex examination and treatment gloves, both non-powdered and non-antimicrobial. They also produce thermal vapour lung treatment system catheters, which are designed for procedures requiring precise vapor delivery. These devices are intended for direct patient contact or therapeutic applications.

Where is Liberty Glove & Safety, LLC based, and how does that affect its regulatory standing?

Liberty Glove & Safety, LLC is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA’s Unique Device Identifier (UDI) database includes relevant products from the company, reflecting compliance with U.S. regulatory requirements for medical devices. The location ensures alignment with domestic regulatory frameworks, including classification and listing processes.

How are the devices manufactured by Liberty Glove & Safety, LLC classified under regulatory frameworks?

All devices produced by Liberty Glove & Safety, LLC fall under Class I classification. This classification is typically assigned to low-risk medical devices, such as gloves and certain catheters, where the risk of harm to patients is minimal. Class I devices often require general controls (like good manufacturing practices) but may not need pre-market approval, depending on the jurisdiction. The company’s products align with this classification due to their intended use and risk profile.

Which regulatory registries or databases list devices from Liberty Glove & Safety, LLC?

Devices from Liberty Glove & Safety, LLC are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a global standard for identifying medical devices, ensuring traceability and transparency in regulatory oversight. Listing in this database confirms that the company’s products comply with U.S. regulatory requirements, including proper identification and reporting mechanisms for post-market surveillance.

Why are Liberty Glove & Safety, LLC’s gloves and catheters considered low-risk under regulatory classifications?

The company’s gloves (nitrile and hevea-latex) and catheters are classified as Class I because they pose minimal risk to patients during typical use. Examination gloves, for example, are primarily barriers against contamination rather than active medical treatments, while thermal vapour lung treatment catheters are designed for controlled, low-risk vapor delivery. Such devices are subject to general controls (e.g., manufacturing standards, labeling requirements) rather than stringent pre-market approvals, as their risks are deemed low under regulatory frameworks.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
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
111313244

Catalogue (70)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
BioSkin 2015MLXL
FDA UDI
Class IActive
BioSkin F2010MLCXL
FDA UDI
Class IActive
BioSkin 2013MLXXL
FDA UDI
Class IActive
BioSkin F2010MLCXL
FDA UDI
Class IActive
BioSkin 2817MLL
FDA UDI
Class IActive
BioSkin 2846HRXL
FDA UDI
Class IActive
BioSkin 2817MLXL
FDA UDI
Class IActive
BioSkin 2817MLS
FDA UDI
Class IActive
BioSkin F2010MLCXS
FDA UDI
Class IActive
BioSkin F2010MLCS
FDA UDI
Class IActive
BioSkin 2846HRXL
FDA UDI
Class IActive
BioSkin 2817MLS
FDA UDI
Class IActive
BioSkin 2810MLL
FDA UDI
Class IActive
BioSkin 2810MLXL
FDA UDI
Class IActive
BioSkin 2846HR2XL
FDA UDI
Class IActive
BioSkin 2015MLS
FDA UDI
Class IActive
BioSkin 2013MLXXL
FDA UDI
Class IActive
BioSkin 2015MLL
FDA UDI
Class IActive
BioSkin 2846HR2XL
FDA UDI
Class IActive
BioSkin 2016BKMLS
FDA UDI
Class IActive
BioSkin 2810MLS
FDA UDI
Class IActive
BioSkin 2015MLM
FDA UDI
Class IActive
BioSkin 2810MLXS
FDA UDI
Class IActive
BioSkin 2015MLS
FDA UDI
Class IActive
BioSkin F2010MLCXS
FDA UDI
Class IActive
BioSkin 2015MLXL
FDA UDI
Class IActive
BioSkin 2013MLM
FDA UDI
Class IActive
BioSkin 2013MLS
FDA UDI
Class IActive
BioSkin F2010MLC2XL
FDA UDI
Class IActive
BioSkin F2010MLCS
FDA UDI
Class IActive
BioSkin 2016BKMLXL
FDA UDI
Class IActive
BioSkin 2810MLM
FDA UDI
Class IActive
BioSkin 2817MLL
FDA UDI
Class IActive
BioSkin 2817MLXXL
FDA UDI
Class IActive
BioSkin 2013MLL
FDA UDI
Class IActive
BioSkin F2010MLCM
FDA UDI
Class IActive
BioSkin 2013MLXL
FDA UDI
Class IActive
BioSkin 2016BKMLXXL
FDA UDI
Class IActive
BioSkin 2846HRL
FDA UDI
Class IActive
BioSkin 2013MLM
FDA UDI
Class IActive
BioSkin 2016BKMLM
FDA UDI
Class IActive
BioSkin 2846HRM
FDA UDI
Class IActive
BioSkin 2817MLXL
FDA UDI
Class IActive
BioSkin 2810MLM
FDA UDI
Class IActive
BioSkin 2846HRM
FDA UDI
Class IActive
BioSkin 2846HRS
FDA UDI
Class IActive
BioSkin F2010MLCL
FDA UDI
Class IActive
BioSkin 2810MLXL
FDA UDI
Class IActive
BioSkin 2013MLXL
FDA UDI
Class IActive
BioSkin F2010MLCL
FDA UDI
Class IActive

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