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LnK Spinal Fixation System 1061-60180

by L&K Biomed Co., Ltd.

LnK Spinal Fixation System 1061-60180 is a Class II device made by L&K Biomed Co., Ltd., listed in FDA GUDID since 15 May 2015 (UDI-DI 08806189844549), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08806189844549 UDI-DI Date15 May 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
LnK Spinal Fixation System
Generic name
Bone-screw internal spinal fixation system rod
Model / Ref / Catalog
1061-60180
Primary DI / UDI-DI
08806189844549
FDA product code
KWP, KWQ, MNH, MNI, NKB
GMDN term
Bone-screw internal spinal fixation system rod
Device class
Class II
Regulation number
888.3050, 888.3060, 888.3070
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-screw internal spinal fixation system rod

Other devices from L&K Biomed

See all devices from L&K Biomed →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)