Data / Medical devices / China / Jinhua Qidian Vehicle Co. Ltd
Jinhua Qidian Vehicle Co. Ltd: FDA-registered device maker in Jinhua Zhejiang, China, 1 510(k) clearance
Jinhua Qidian Vehicle Co. Ltd is registered with the FDA (registration 3043105164) in Jinhua Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 20, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043105164
- Address
- #8.NO308. WeiyeRoad, Jiangtang, Wucheng, Jinhua Zhejiang, China, 321000
- Owner or operator
- Jinhua Qidian Vehicle Co. Ltd (10094604)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- December 10, 2025
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair (qdwp-a01, qdwp-b02)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| June 20, 2025 | K251248 | ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) | ITI | Substantially Equivalent | Jinhua Qidian Vehicle Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 20, 2025. 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.