Data / Medical devices / China / Nanjing MIJO Technology Co., Ltd
Nanjing MIJO Technology Co., Ltd: FDA-registered device maker in Nanjing Jiangsu, China, 2 510(k) clearances
Nanjing MIJO Technology Co., Ltd is registered with the FDA (registration 3042262539) in Nanjing Jiangsu, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 29, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3042262539
- Address
- Building A3-2, Yongning Intelligent Manufacturing Industrial Park, No. 77 Hupo Road, Nanjing Jiangsu, China, 210000
- Owner or operator
- Nanjing MIJO Technology Co., Ltd (10094277)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- November 20, 2025
- Registered through
- 2027
- Brand names listed
- Power Mobility Scooter (MA03), Power Mobility Scooter (MJMA01, MJMA02), Walking Stick
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cane, Safety Walk | KHY | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| September 29, 2026 | K262213 | Power Mobility Scooter (MA03) | INI | Substantially Equivalent | Nanjing Mijo Technology Co., Ltd. | accessdata.fda.gov |
| March 12, 2026 | K253936 | Power Mobility Scooter (MJMA01, MJMA02) | INI | Substantially Equivalent | Nanjing Mijo Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 29, 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.