CastleLoc-C Cervical Interbody Fusion Cage System

Cervical Cage 14, 17, 05mm 0°

Registry build 21.09.26
7manufacturers in China registered for this device type
54catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for CastleLoc-C Cervical Interbody Fusion Cage System
Listed by L&K Biomed Co., Ltd., South Korea
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer, Exporter
510(k) K151677
Record published 2017-09-20
Record revised 2020-02-24 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for CastleLoc-C Cervical Interbody Fusion Cage System
Catalogue number Size Status
5105-1417 In distribution
5108-1519 In distribution
5109-1417 In distribution
5107-1517 In distribution
5109-1217 In distribution
5107-1217 In distribution
5105-1419 In distribution
5106-1419 In distribution
5106-1315 In distribution
5108-1417 In distribution
5106-1414 In distribution
5110-1417 In distribution
5109-1315 In distribution
5107-1515 In distribution
5109-1414 In distribution
5109-1515 In distribution
5107-1414 In distribution
5109-1419 In distribution
5109-1517 In distribution
5110-1517 In distribution
5106-1515 In distribution
5108-1515 In distribution
5109-1519 In distribution
5109-1214 In distribution
5105-1315 In distribution
5106-1214 In distribution
5108-1419 In distribution
5110-1214 In distribution
5106-1217 In distribution
5107-1419 In distribution
5107-1417 In distribution
5108-1517 In distribution
5110-1519 In distribution
5107-1214 In distribution
5110-1315 In distribution
5106-1417 In distribution
5108-1315 In distribution
5105-1217 In distribution
5105-1414 In distribution
5107-1519 In distribution
5110-1515 In distribution
5105-1519 In distribution
5106-1519 In distribution
5108-1214 In distribution
5105-1214 In distribution
5105-1517 In distribution
5107-1315 In distribution
5105-1515 In distribution
5110-1419 In distribution
5110-1414 In distribution
5108-1217 In distribution
5106-1517 In distribution
5110-1217 In distribution
5108-1414 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K262489 2026-08-18
K260840 2026-05-16
K151677 2015-07-15
K143360 2015-04-03
K120840 2012-05-24

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer