Akers w104

by Akers Industries, Inc.

Akers w104 is a Class I device made by Akers Industries, Inc., listed in FDA GUDID since 20 Oct 2022 (UDI-DI 00759326227133), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00759326227133 UDI-DI	Date20 Oct 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00759326227133

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Akers
Generic name: Vinyl examination/treatment glove, non-powdered
Model / reference: w104

Primary DI / UDI-DI: 00759326227133
FDA product code: LYZ
GMDN term: Vinyl examination/treatment glove, non-powdered

Device class: Class I
Regulation number: 880.6250
GUDID distribution status: In Commercial Distribution

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Other devices filed under Vinyl examination/treatment glove, non-powdered.

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Properties

Single use
Lot / batch number
Expiration date
Manufacturing date

Other properties (11, all answered No)