Data / Medical devices / System, Ablation, Microwave And Accessories / China
FDA-registered makers of System, Ablation, Microwave And Accessories in China: 8 establishments
8 establishments in China are registered with the FDA to make System, Ablation, Microwave And Accessories (product code NEY). 8 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- System, Ablation, Microwave And Accessories
- Product code
- NEY
- Country
- China
Makers of System, Ablation, Microwave And Accessories in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Betters(Suzhou) Medical Co., LTD | Suzhou Jiangsu, China | Manufacturer | 2 | November 13, 2023 | 0 | 0 | 0 | api.fda.gov |
| Canyon Medical Inc. | Nanjing Jiangsu, China | Manufacturer | 2 | September 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Covidien Medical Products (Shanghai) Manufacturing LLC | Shanghai, China | Manufacturer | 2 | December 6, 2016 | 0 | 1 | 0 | api.fda.gov |
| ECO Medical Technology (Nanjing) Co., Ltd. | Nanjing Jiangsu, China | Exporter to the US, Manufacturer | 2 | July 23, 2021 | 0 | 0 | 0 | api.fda.gov |
| Nanjing Devin Medical Technology Co., Ltd. | Nanjing Jiangsu, China | Manufacturer | 2 | March 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Hygea Medical Technology Co., Ltd. | Beijing, China | Manufacturer | 1 | January 31, 2024 | 0 | 0 | 0 | api.fda.gov |
| Mima-Pro (nan Tong) Scientific Inc. | Nantong Jiangsu, China | Manufacturer | 1 | February 28, 2023 | 0 | 0 | 0 | api.fda.gov |
| Surgnova Healthcare Technologies (zhejiang) Co., Ltd. | Cixi Zhejiang, China | Manufacturer | 1 | July 8, 2019 | 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.