Perfix™ Spinal System

17 catalogue numbers from SG1640, listed by CG MedTech Co., Ltd., South Korea, under Orthosis, Spinal Pedicle Fixation. 13 manufacturers in China are registered for this product code.

Registry build 21.09.26
13manufacturers in China registered for this device type
17catalogue 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 MNI
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, Spinal Pedicle Fixation

Record

Regulatory record for Perfix™ Spinal System
Listed by CG MedTech Co., Ltd., South Korea
FDA product code MNI
Device type Orthosis, Spinal Pedicle Fixation
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Complaint-file establishment, Manufacturer
510(k) K020279
Record published 2023-02-25
Record revised 2025-07-02 (version 4)

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, serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Perfix™ Spinal System
Catalogue number Size Status
SG1640 In distribution
SG1620 In distribution
SG1606 In distribution
SG1660 In distribution
SG1615 In distribution
SG1648 In distribution
SG1610 In distribution
SG1608 In distribution
SG1607 In distribution
SGA2433 In distribution
SG1612 In distribution
SG1630 In distribution
SGA2460 In distribution
SG1605 In distribution
SP3020 In distribution
SG1604 In distribution
SG1609 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. 2,342
Creo Globus Medical, Inc. 1,784
ReLine Nuvasive, Inc. 1,718
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 1,525
Apex Spine System Spinecraft LLC 1,114
Revere Globus Medical, Inc. 1,051
LnK Spinal Fixation System L&K Biomed Co., Ltd. 974
LnK Basic Spinal Fixation System L&K Biomed Co., Ltd. 935
Arsenal Alphatec Spine, Inc. 932
Zavation Zavation 864
Polaris™ 5.5 Spinal System Biomet Spine 809
Apex-DL Spine System Spinecraft LLC 792

Showing 12 of 950. All products under Orthosis, Spinal Pedicle Fixation

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Perfix™ Spinal System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
U&I Corp., America 510(k) number 2004-08-10 Not classified Other Threads on a set screw, as a component of a spinal fixation system, may break off during use. 200 set screws 2005-11-29
U&I Corp., America 510(k) number 2004-01-14 Not classified Other Reports of hex driver tips breaking off or becoming worn or stripped. 320 units 2004-03-24
U&I Corp., America 510(k) number 2004-01-14 Not classified Other Reports of hex driver tips breaking off or becoming worn or stripped. 300 units 2004-03-24
U&I Corp., America 510(k) number 2003-08-18 Not classified Other Reports of pieces chipping off the tip of screwdriver during use. 215 units. 2003-11-19

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