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LnK Spinal Instrument System

FDA UDI

Class I (US FDA UDI)

by L&K Biomed Co. , Ltd.

Identity

Trade Name
LnK Spinal Instrument System FDA UDI
Generic Name
Orthopaedic chisel FDA UDI
Device Name
BOX CHISEL 6H 22MMW/ANGLED FDA UDI
Model / Reference
LC04-0605A FDA UDI
Description
BOX CHISEL 6H 22MMW/ANGLED FDA UDI

Identifiers

Catalog Number
LC04-0605A FDA UDI
Primary DI / UDI-DI
08800108667448 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic chisel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic chisel

LnK Spinal Instrument System by L&K Biomed Co. , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
L&K Biomed Co. , Ltd.

Sources (1)

  • FDA UDI 2829cf08-50d6-4c5a-9a59-67fd14271866 34 fields · synced May 30, 2026