Data / Medical devices / Orthosis, Spondylolisthesis Spinal Fixation / China
FDA-registered makers of Orthosis, Spondylolisthesis Spinal Fixation in China: 11 establishments
11 establishments in China are registered with the FDA to make Orthosis, Spondylolisthesis Spinal Fixation (product code MNH). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Orthosis, Spondylolisthesis Spinal Fixation
- Product code
- MNH
- Country
- China
Makers of Orthosis, Spondylolisthesis Spinal Fixation in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Suzhou Kangli Orthopaedics Instrument Co., Ltd. | Zhangjiagang City Jiangsu, China | Manufacturer | 2 | November 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Ideal Medical Science & Technology Co., Ltd. | Zhangjiagang City Jiangsu, China | Manufacturer | 1 | January 30, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd | Changzhou Jiangsu, China | Manufacturer | 1 | September 27, 2000 | 0 | 0 | 0 | api.fda.gov |
| Shandong Weigao Orthopaedic Device Co.,ltd | weihai Shandong, China | Contract manufacturer, Manufacturer | 1 | April 12, 2013 | 0 | 0 | 0 | api.fda.gov |
| APS Materials Suzhou | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changzhou Yonghua Medical Instruments Co.,ltd | Changzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Synthes (suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Double Medical Technology Inc. | Xiamen Fujian, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Sanyou Medical Co. Ltd | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zibo Dante Co, Ltd | Zibo City Shandong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.