Reliant

108MM Four Level Cervical Plate Assembly, Reliant Acps

Registry build 21.09.26
14manufacturers in China registered for this device type
52catalogue numbers in this listing
1510(k) clearance
1recall

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 Reliant
Listed by Orthofix US LLC, United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K030595
Record published 2019-03-19
Record revised 2026-02-20 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Reliant
Catalogue number Size Status
64-6704 In distribution
64-6108 In distribution
64-6700 In distribution
64-6240 In distribution
64-6116 In distribution
64-6820 In distribution
64-6640 In distribution
64-6340 In distribution
450242-0001 In distribution
64-6120 In distribution
64-6500 In distribution
64-6764 In distribution
64-6540 In distribution
450241-0002 In distribution
64-6580 In distribution
64-6220 In distribution
64-6680 In distribution
64-6300 In distribution
64-6860 In distribution
64-6523 In distribution
64-6260 In distribution
64-6200 In distribution
64-6420 In distribution
64-6724 In distribution
64-6740 In distribution
64-6620 In distribution
64-6280 In distribution
64-6664 In distribution
64-6684 In distribution
64-6844 In distribution
64-6480 In distribution
64-6600 In distribution
64-6440 In distribution
64-6744 In distribution
64-6660 In distribution
64-6884 In distribution
64-6460 In distribution
64-6380 In distribution
64-6360 In distribution
64-6520 In distribution
64-6560 In distribution
64-6112 In distribution
64-6780 In distribution
64-6964 In distribution
64-6320 In distribution
64-6400 In distribution
64-6804 In distribution
64-6104 In distribution
64-6924 In distribution
64-6100 In distribution
64-6543 In distribution
64-6900 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
K211712 2022-02-11

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-10-29 Class II Component design/selection There is a possibility that the locking mechanism of the Azure Anterior Cervical Plate may fracture during or after implantation. 4,172 units 2014-12-09

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