Super Source GLO529BK

by Super Source

Super Source GLO529BK is a Class I device made by Super Source, listed in FDA GUDID since 30 May 2025 (UDI-DI 10850020042217), 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	Number10850020042217 UDI-DI	Date30 May 2025Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10850020042217

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Super Source
Generic name: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference: GLO529BK

Primary DI / UDI-DI: 10850020042217
FDA product code: LZA
GMDN term: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

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

Other devices from Super Source

See all devices from Super Source →

Properties

Single use
Over-the-counter
Premarket exempt

Other properties (12, all answered No)