Data / Medical devices / China / Zhejiang Automwheel Tech Co., Ltd
Zhejiang Automwheel Tech Co., Ltd: FDA-registered device maker in Jinhua City Zhejiang, China, 1 510(k) clearance
Zhejiang Automwheel Tech Co., Ltd is registered with the FDA (registration 3043711862) in Jinhua City Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 2, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043711862
- Address
- No. 99 Qingya Rd, Feiyang Town, Jinhua City Zhejiang, China, 321025
- Owner or operator
- Zhejiang Automwheel Tech Co., Ltd (10095071)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- January 21, 2026
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair AT-001
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 |
|---|---|---|---|---|---|---|
| July 2, 2025 | K251285 | Electric Wheelchair (HG-630) | ITI | Substantially Equivalent | Zhejiang Automwheel Tech Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 2, 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.