Data / Medical devices / Accelerator, Linear, Medical / China
FDA-registered makers of Accelerator, Linear, Medical in China: 10 establishments
10 establishments in China are registered with the FDA to make Accelerator, Linear, Medical (product code IYE). 7 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
- Accelerator, Linear, Medical
- Product code
- IYE
- Country
- China
Makers of Accelerator, Linear, Medical in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Klarity Medical & Equipment (GZ) Co., Ltd. | Guangzhou Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 5 | March 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Varian Medical Systems China Co., Ltd. | Beijing, China | Manufacturer | 4 | January 21, 2026 | 0 | 0 | 0 | api.fda.gov |
| Beijing LinaTech Medical Technology Co. Ltd | Beijing, China | Exporter to the US, Manufacturer | 3 | April 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Manteia Technologies Co.,ltd. | Xiamen Fujian, China | Manufacturer | 2 | October 24, 2025 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Rayer Medical Technology Co., Ltd. | Wuxi Jiangsu, China | Manufacturer | 1 | May 1, 2020 | 0 | 0 | 0 | api.fda.gov |
| Our United Corporation | Xian Shaanxi, China | Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer | 1 | August 7, 2020 | 0 | 0 | 0 | api.fda.gov |
| Wisdom Technologies, Inc. | Hefei Anhui, China | Manufacturer | 1 | January 5, 2024 | 0 | 0 | 0 | api.fda.gov |
| Dalian Sportech Apparel Co., Ltd | Dalian Liaoning, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Elekta Beijing Medical Systems Co., Ltd | Beijing, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou Tian Hong Medical Technology Co., Ltd. | Guangzhou Guangdong, 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.