Data / Medical devices / China / Nanjing Devin Medical Technology Co., Ltd.
Nanjing Devin Medical Technology Co., Ltd.: FDA-registered device maker in Nanjing Jiangsu, China, 2 510(k) clearances
Nanjing Devin Medical Technology Co., Ltd. is registered with the FDA (registration 3045005759) in Nanjing Jiangsu, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 2, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045005759
- Address
- Building 9, 3rd Floor, No. 86, Shuanggao Road, Economic Development Zone, Gaochun District, Nanjing Jiangsu, China, 211300
- Owner or operator
- Nanjing Devin Medical Technology Co., Ltd. (10095519)
- Roles
- Manufacturer
- First device listed
- March 24, 2026
- Registered through
- 2026
- Brand names listed
- Disposable Microwave Ablation Antenna, Microwave Ablation Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Ablation, Microwave And Accessories | NEY | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 2, 2026 | K253771 | Disposable Microwave Ablation Antenna (DW-XR-II1, DW-XR-II3, DW-XR-II4, DW-XR-II14, DW-XR-II5, DW-XR-II6, DW-XR-II7, DW-XR-II8, DW-XR-II9, DW-XR-II10, DW-XR-II18, DW-XR-II19, DW-XR-II20, DW-XR-II21, DW-DG-II6, DW-DG-II7, DW-DG-II9, DW-DG-II10, DW-DG-II13) | NEY | Substantially Equivalent | Nanjing Devin Medical Technology Co., Ltd. | accessdata.fda.gov |
| March 2, 2026 | K252632 | Microwave Ablation Device | NEY | Substantially Equivalent | Nanjing Dewen Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 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.