ForPro 140736

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

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	Number00672047000246 UDI-DI	Date10 Nov 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK102444	Date22 Nov 2010Decided	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Withdrawn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: Vinyl examination/treatment glove, non-powdered
Model / reference: 140736
Description: Vinyl Exam Gloves SIze X-Large 100ct

Primary DI / UDI-DI: 00672047000246
510(k) Number: K102444
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 Tng Worldwide Inc

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ForPro 140792

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ForPro 140796

Class I
ForPro 140798

Class I
ForPro 140704

Class I
ForPro 140740

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