Matrix

9.0MM TI Cann Matrix Polyaxial Screw 65MM Thread Length

Registry build 21.09.26
13manufacturers in China registered for this device type
45catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNH
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
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
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Changzhou Yonghua Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 8
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7

Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spondylolisthesis Spinal Fixation

Record

Regulatory record for Matrix
Listed by Synthes Gmbh, Switzerland
FDA product code MNH
Device type Orthosis, Spondylolisthesis Spinal Fixation
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Manufacturer, Exporter
510(k) K092929
Record published 2015-09-14
Record revised 2025-07-14 (version 6)

Specifications

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

Catalogue Numbers

Catalogue numbers for Matrix
Catalogue number Size Status
04.632.650 In distribution
04.632.830 In distribution
04.632.725 In distribution
04.632.000 In distribution
04.632.640 In distribution
04.632.965 In distribution
04.634.420 In distribution
04.639.799 In distribution
04.639.770 In distribution
04.634.750 In distribution
04.634.430 In distribution
04.634.440 In distribution
04.632.540 In distribution
04.639.120 In distribution
04.606.965 In distribution
04.632.665 In distribution
04.639.430 In distribution
04.632.130 In distribution
04.639.855 In distribution
04.634.435 In distribution
04.634.645 In distribution
04.634.825 In distribution
04.606.625 In distribution
04.606.765 In distribution
04.634.635 In distribution
04.606.550 In distribution
04.616.525 In distribution
04.639.725 In distribution
04.639.520 In distribution
04.639.625 In distribution
04.632.001 In distribution
04.634.845 In distribution
04.632.140 In distribution
04.639.675 In distribution
04.634.520 In distribution
04.639.145 In distribution
04.632.980 In distribution
04.639.755 In distribution
04.616.840 In distribution
04.639.775 In distribution
04.606.835 In distribution
04.639.550 In distribution
04.632.675 In distribution
04.606.660 In distribution
04.606.725 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 3,144
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 2,177
ReLine Nuvasive, Inc. 2,010
Creo Globus Medical, Inc. 1,619
Perfix™ Spinal System CG MedTech Co., Ltd. 1,476
Apex Spine System Spinecraft LLC 1,193
Olympic Astura Medical 1,173
Arsenal Alphatec Spine, Inc. 1,001
Revere Globus Medical, Inc. 997
Astra Spine System Spinecraft LLC 798
Apex-DL Spine System Spinecraft LLC 735
Zenius Spinal System Medyssey Co., Ltd. 712

Showing 12 of 811. All products under Orthosis, Spondylolisthesis Spinal Fixation

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Matrix
Recalled by Identified by Initiated FDA class Root cause Reason Closed
Synthes USA (HQ), Inc. 510(k) number 2011-03-11 Not classified Labeling Change Control Labeling Correction — The locking cap was not able to be loosened, resulting in the breakage of the screwdriver or the rod to be cut and the assembly to be removed (screw, cap, and rod). This poses a potential risk of significant prolonga 2014-12-18

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