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Medline Industires, Inc.

Also registered as Medline Industires, LP

United StatesFDA applicant, unverified

Devices
6

What Medline Industires, Inc. makes

Medline Industries, Inc. manufactures single-use medical gloves, including powder-free nitrile examination gloves tested for use with chemotherapy drugs, as well as a variable-concentration large-volume nebulizer for respiratory therapy. The company also produces orthopedic fixation hardware, such as the Jones Fracture Screw System, and a smoke evacuation device for surgical procedures.

The company’s products are regulated under FDA’s Class I and Class II categories, with several devices cleared via the 510(k) pathway. These items are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Medline Industires, Inc. have in the registry?

The registry currently lists 6 devices for Medline Industires, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medline Industires, Inc.'s devices?

Among its 6 most recently registered devices, Medline Industires, Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Medline Industires, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Medline Industires, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medline Industires, Inc. in the registry?

The most recently registered devices listed for Medline Industires, Inc. include Medline Powder Free Examination Gloves (Tested for use with Chemotherapy Drugs), Medline Powder-Free Light Blue Nitrile Exam Gloves (Tested for Use with Chemotherapy Drugs), Hudson RCI Variable concentration Large Volume Nebulizer (1770) and Medline UNITE Jones Fracture Screw System.

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