Truline A142343

by Arbill Industries, Inc. 2 variants

Truline A142343 is a Class I device made by Arbill Industries, Inc., cleared under FDA 510(k) K133307 and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 10850052602106), active as of 23 Oct 2026.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K133307↗

FDA submission, from GUDID

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	Number10850052602106 UDI-DI	Date8 Jun 2023Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k) from GUDID	NumberK133307	Date—	StatusActive

Official records

AccessGUDID record UDI-DI 10850052602106
FDA 510(k) database 510(k) number K133307

Across registries

2 registries list this device

FDA 510(k) K133307 Active
FDA GUDID UDI-DI 10850052602106 listed 8 Jun 2023 Listed

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Truline
Generic name: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference: A142343

Primary DI / UDI-DI: 10850052602106
510(k) Number: K133307
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 Arbill Industries, Inc.

Truline A122344

Class I
Truline A112344

Class I
Truline A112353

Class I
Truline A155021

Class I

See all devices from Arbill Industries, Inc. →

Properties

Single use

Other properties (14, all answered No)