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CastleLoc-S Posterior Cervical Fixation System/LnK Posterior Cervical Fixation S

FDA UDI

Class II (US FDA UDI)

by L&K Biomed Co. , Ltd.

Identity

Trade Name
CastleLoc-S Posterior Cervical Fixation System/LnK Posterior Cervical Fixation S FDA UDI
Generic Name
Bone-screw internal spinal fixation system connector FDA UDI
Device Name
Lateral Connector FDA UDI
Model / Reference
6144-0019 FDA UDI
Description
Lateral Connector FDA UDI

Identifiers

Catalog Number
6144-0019 FDA UDI
Primary DI / UDI-DI
08806344322585 FDA UDI
FDA Product Code
NKG FDA UDI
KWP FDA UDI
GMDN Term
Bone-screw internal spinal fixation system connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3075 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system connector

CastleLoc-S Posterior Cervical Fixation System/LnK Posterior Cervical Fixation S by L&K Biomed Co. , Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bone-screw internal spinal fixation system connector.

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 769c9e88-7289-4664-bdaa-ac3d0486609b 34 fields · synced May 30, 2026