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LnK Spinal Instrument System LC04-CM05

by L&K Biomed Co., Ltd.

Ref LC04-CM05

LnK Spinal Instrument System LC04-CM05 is a Class I device made by L&K Biomed Co., Ltd., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI B-08800108674637) and listed in FDA GUDID since 24 Jul 2024 (UDI-DI 08800108674637), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08800108674637 Basic UDI-DI 08800108674637UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08800108674637 UDI-DI Date24 Jul 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08800108674637 registered 31 Oct 2026 Active
  • FDA GUDID UDI-DI 08800108674637 listed 24 Jul 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08800108674637
  2. Registered EUDAMED B-08800108674637

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
LnK Spinal Instrument System
Generic name
Bone curette, reusable
Model / Ref / Catalog
LC04-CM05
Primary DI / UDI-DI
08800108674637
Basic UDI-DI
B-08800108674637
FDA product code
LXH
EMDN code
L0901 Orthopaedic surgery spoons and curettes, reusable
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
888.4540
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE.

Other devices from L&K Biomed

See all devices from L&K Biomed →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
Other properties (20, all answered No)