Coalition AGX

COALITION AGX Plate, 14mm W, 11mm H

Registry build 21.09.26
14manufacturers in China registered for this device type
32catalogue numbers in this listing
15510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for Coalition AGX
Listed by Globus Medical, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Manufacturer, Exporter
510(k) K142218
Record published 2015-11-07
Record revised 2025-07-14 (version 5)

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
Sizes Height 5 to 12 mm; width 14 to 20 mm

Catalogue Numbers

Catalogue numbers for Coalition AGX
Catalogue number Size Status
1128.1211 Height 11 mm In distribution
1128.1409 Height 9 mm In distribution
1128.1407 Width 16 mm In distribution
1128.1205 Height 5 mm In distribution
1128.1505 Height 5 mm In distribution
1128.1530 Height 10 mm In distribution
1128.1405 Width 16 mm In distribution
1128.1506 Width 18 mm In distribution
1128.1206 Height 6 mm In distribution
1128.1528 Width 20 mm In distribution
1128.1510 Width 18 mm In distribution
1128.1531 Width 20 mm In distribution
1128.1408 Width 16 mm In distribution
1128.1411 Width 16 mm In distribution
1128.1532 Height 12 mm In distribution
1128.1207 Height 7 mm In distribution
1128.1512 Height 12 mm In distribution
1128.1406 Width 16 mm In distribution
1128.1412 Height 12 mm In distribution
1128.1511 Height 11 mm In distribution
1128.1208 Height 8 mm In distribution
1128.1525 Width 20 mm In distribution
1128.1509 Width 18 mm In distribution
1128.1410 Width 16 mm In distribution
1128.1508 Height 8 mm In distribution
1128.1527 Height 7 mm In distribution
1128.1210 Width 14 mm In distribution
1128.1507 Height 7 mm In distribution
1128.1212 Height 12 mm In distribution
1128.1526 Height 6 mm In distribution
1128.1529 Width 20 mm In distribution
1128.1209 Height 9 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233735 2024-01-25
K232318 2023-10-31
K192314 2019-10-23
K183056 2019-04-19
K181846 2018-11-06
K133567 2014-02-20
K121049 2012-06-27
K120092 2012-04-13
K092146 2009-11-16
K092108 2009-08-13
K081391 2008-07-03
K070775 2007-04-19
K062836 2006-12-19
K062407 2006-09-06
K040721 2004-06-17

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