Data / Medical devices / China / Yongkang Hengyi Vehicle Co.,ltd
Yongkang Hengyi Vehicle Co.,ltd: FDA-registered device maker in Jinhua Zhejiang, China, 2 510(k) clearances
Yongkang Hengyi Vehicle Co.,ltd is registered with the FDA (registration 3035853002) in Jinhua Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 8, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035853002
- Address
- NO.225 Xishan Road, Yongkang Economic Development Zone, Jinhua Zhejiang, China, 321300
- Owner or operator
- Yongkang Hengyi Vehicle Co.,Ltd (10092435)
- Roles
- Manufacturer
- First device listed
- January 7, 2025
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair (HC820N), Electric wheelchair (HC819N, HC830N, HC831N), Rollator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Walker, Mechanical | ITJ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| September 8, 2026 | K260229 | Electric wheelchair (HC819N, HC830N, HC831N) | ITI | Substantially Equivalent | Yongkang Hengyi Vehicle Co., Ltd. | accessdata.fda.gov |
| December 19, 2024 | K243440 | Electric Wheelchair (HC820N) | ITI | Substantially Equivalent | Yongkang Hengyi Vehicle Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 8, 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.