Skintx 70010

by Gd Care Inc.

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

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB75470010 UDI-DI	Date29 Sep 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Skintx
Generic name: Vinyl examination/treatment glove, non-powdered
Model / reference: 70010

Primary DI / UDI-DI: B75470010
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

Other devices from Gd Care Inc.

Great Glove SBLK-NM515E

Class I
Great Glove NM50015E

Class I
Skintx 50020

Class I
Skintx 90015FIT

Class I
Care CBK9-515

Class I
Care CS-510

Class I

See all devices from Gd Care Inc. →

Properties

Single use
Over-the-counter
Lot / batch number
Serial number
Manufacturing date

Other properties (10)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Contains latex: No
Prescription use: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Expiration date: No