ForPro 140704

by Tng Worldwide Inc

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 22 Oct 2026

Documents

510(k) K110981↗

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00672047204774 UDI-DI	Date12 Jan 2023Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k) from GUDID	NumberK110981	Date—	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: ForPro
Generic name: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference: 140704
Description: Black Nitrile Glove Size Large 1000ct

Primary DI / UDI-DI: 00672047204774
510(k) Number: K110981
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 Tng Worldwide Inc

ForPro 140794

Class I
ForPro 140792

Class I
ForPro 140796

Class I
ForPro 140798

Class I
ForPro 140740

Class I
ForPro 140664

Class I

See all devices from Tng Worldwide Inc →

Properties

Single use
Over-the-counter

Other properties (13)

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
Lot / batch number: No
Serial number: No
Expiration date: No
Manufacturing date: No