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Elite International, Inc.

US

Last updated May 23, 2026

What Elite International, Inc. makes

Elite International, Inc. manufactures disposable vinyl exam gloves, including powdered and powder-free variants. The powder-free line includes formulations with added vitamin complexes, nopal, and lanolin. These gloves are designed for single-use medical and clinical examinations.

The company’s products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. 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 Elite International, Inc. manufacture?

Elite International, Inc. specializes in disposable vinyl exam gloves. Their product line includes both powdered and powder-free versions, with some powder-free gloves featuring additional ingredients like vitamin complexes, nopal, and lanolin. These gloves are intended for single-use medical and clinical examinations.

Where is Elite International, Inc. based?

Elite International, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, as it operates within the FDA’s jurisdiction.

How are Elite International, Inc.’s devices classified under FDA regulations?

Elite International, Inc.’s disposable vinyl exam gloves are classified as Class I medical devices by the FDA. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, allowing for streamlined regulatory oversight.

Are Elite International, Inc.’s devices listed in any regulatory registries?

Yes, Elite International, Inc.’s devices are listed via the FDA’s 510(k) clearance pathway. This process demonstrates that the manufacturer has shown their products are substantially equivalent to a legally marketed predicate device, meeting FDA requirements for marketing authorization.

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

Information

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US
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Catalogue (581)

Page 9 of 12
DeviceModel / ReferenceRegistriesClassStatus
Bevel 8696BCBK
FDA UDI
Class IActive
Bevel 8741TGBM
FDA UDI
Class IActive
Bevel 8702DGDB
FDA UDI
Class IActive
Bevel 2552BPBH
FDA UDI
Class IActive
Bevel 8735WHPB
FDA UDI
Class IActive
Bevel 8740BSGB
FDA UDI
Class IActive
Bevel 3724SC
FDA UDI
Class IActive
Bevel 6536DSSB
FDA UDI
Class IActive
Bevel 8668RDPC
FDA UDI
Class IActive
Bevel 8726BUDB
FDA UDI
Class IActive
Bevel 8668BOLB
FDA UDI
Class IActive
Bevel 8734CUSY
FDA UDI
Class IActive
Bevel 2547BG
FDA UDI
Class IActive
Bevel 8716BUGG
FDA UDI
Class IActive
Bevel 3690ORB
FDA UDI
Class IActive
Bevel 3725TUM
FDA UDI
Class IActive
Bevel 3638BM
FDA UDI
Class IActive
Bevel 8652BBGR
FDA UDI
Class IActive
Bevel 3648LG
FDA UDI
Class IActive
Bevel 3721MO
FDA UDI
Class IActive
Bevel 8714MGST
FDA UDI
Class IActive
Bevel 8733BCDI
FDA UDI
Class IActive
Bevel 6546PLCO
FDA UDI
Class IActive
Bevel 8727TGLV
FDA UDI
Class IActive
Bevel 3730PCF
FDA UDI
Class IActive
Bevel 3717PK
FDA UDI
Class IActive
Bevel 6543GTWR
FDA UDI
Class IActive
Bevel 8679DISY
FDA UDI
Class IActive
Bevel 3648RD
FDA UDI
Class IActive
Bevel 3723NC
FDA UDI
Class IActive
Bevel 3722NC
FDA UDI
Class IActive
Bevel 3726BPG
FDA UDI
Class IActive
Bevel 8726PWBU
FDA UDI
Class IActive
Bevel 3729BG
FDA UDI
Class IActive
Bevel 3727SL
FDA UDI
Class IActive
Bevel 8652DGIB
FDA UDI
Class IActive
Bevel 8738GTWR
FDA UDI
Class IActive
Bevel 6546MBDP
FDA UDI
Class IActive
Bevel 3717WS
FDA UDI
Class IActive
Bevel 8705PHST
FDA UDI
Class IActive
Bevel 6536MBDP
FDA UDI
Class IActive
Bevel 2545ES
FDA UDI
Class IActive
Bevel 3727AQ
FDA UDI
Class IActive
Bevel 6537CPMA
FDA UDI
Class IActive
Bevel 2540MBM
FDA UDI
Class IActive
Bevel 3717SC
FDA UDI
Class IActive
Bevel 2545TG
FDA UDI
Class IActive
Bevel 6542WREG
FDA UDI
Class IActive
Bevel 8729BUDB
FDA UDI
Class IActive
Bevel 6543WREG
FDA UDI
Class IActive

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