Data / Medical devices / Appliance, Fixation, Spinal Intervertebral Body / China
FDA-registered makers of Appliance, Fixation, Spinal Intervertebral Body in China: 11 establishments
11 establishments in China are registered with the FDA to make Appliance, Fixation, Spinal Intervertebral Body (product code KWQ). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Appliance, Fixation, Spinal Intervertebral Body
- Product code
- KWQ
- Country
- China
Makers of Appliance, Fixation, Spinal Intervertebral Body in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shanghai Sanyou Medical Co. Ltd | Shanghai, China | Manufacturer | 2 | October 5, 2017 | 0 | 0 | 0 | api.fda.gov |
| Double Medical Technology Inc. | Xiamen Fujian, China | Manufacturer | 1 | March 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd | Changzhou Jiangsu, China | Manufacturer | 1 | November 1, 2007 | 0 | 0 | 0 | api.fda.gov |
| Shandong Weigao Orthopaedic Device Co.,ltd | weihai Shandong, China | Contract manufacturer, Manufacturer | 1 | February 1, 2013 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Decans Medical Devices Co.,ltd. | Jiaxing Zhejiang, China | Manufacturer | 1 | May 14, 2026 | 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 | |
| Depuy Synthes (suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LX Precision Shanghai Co Ltd | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou Jiangsu, China | Contract 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 2, 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.