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Uline, Inc.

United Statesfrom the FDA registration address FDA FEI 3002661124

Uline, Inc. is a medical device manufacturer, with 188 devices listed in FDA GUDID (FDA Class I, Unclassified and Class II) as of 13 Nov 2026.

Devices
188
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 188
Device classes
  • FDA Class I 140
  • FDA Unclassified 41
  • FDA Class II 7
Identifiers
  • FDA FEI 3002661124
  • DUNS 039612668

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Uline, Inc. makes

The company manufactures single-use medical gloves (nitrile and latex, non-powdered and non-antimicrobial), first aid supplies (medicated kits and fingertip bandages), hearing protection (corded and uncorded earplugs), isolation gowns, surgical/medical face masks, and skin-cover adhesive strips. Products include examination gloves, bloodborne pathogen kits, and wall-mounted storage solutions for contaminated items.

These devices are regulated under FDA’s Class I and Class II classifications, with some listed as exempt (Class N or U). They are included in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue188

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Company details

FDA FEI number
3002661124
DUNS number
039612668
Address
12575 Uline Dr, Pleasant Prairie, WI, 53158

Frequently asked questions

How many devices does ULINE, INC. have in the registry?

The registry currently lists 188 devices for ULINE, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ULINE, INC.'s devices?

Among its 50 most recently registered devices, ULINE, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do ULINE, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for ULINE, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from ULINE, INC. in the registry?

The most recently registered devices listed for ULINE, INC. include Trauma Kit H-9954, ULINE BLACK EXAM NITRILE GLVS-L S-21081-L, ULINE BLACK EXAM NITRILE GLVS-S S-21081-S and ULINE BLACK EXAM NITRILE GLVS-M S-21081-M.

Generated automatically from registry data and not verified by a human reviewer.