Counter Torque ST 83142N

by Premia Spine Ltd

Counter Torque ST 83142N is a Class II device made by Premia Spine Ltd, listed in FDA GUDID since 25 May 2026 (UDI-DI 07290115935615), registry data as of 22 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07290115935615 UDI-DI	Date25 May 2026Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 07290115935615

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Counter Torque ST
Generic name: Orthopaedic counter-torque/rod-pushing instrument
Model / reference: 83142N

Primary DI / UDI-DI: 07290115935615
FDA product code: NKB, MNI, MNH, QWK
GMDN term: Orthopaedic counter-torque/rod-pushing instrument

Device class: Class II
Regulation number: 888.3070
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Class II

See all devices from Premia Spine Ltd →

Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)

Regulatory status

Coverage

Specification

Other devices from Premia Spine Ltd

XL Adaptor 87146 Open recall

XL Screwdriver CM 89197 Open recall

Screwdriver CM 89173 Open recall

Tube for K-wire over a k-wire technique 470mm (Nitinol) 89289 Open recall

Properties