Data / Medical devices / China / Ningbo Youhuan Automation Technology Co., Ltd.
Ningbo Youhuan Automation Technology Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 2 510(k) clearances
Ningbo Youhuan Automation Technology Co., Ltd. is registered with the FDA (registration 3035782854) in Ningbo Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 26, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035782854
- Address
- Room 103-24, No.352 Tai'an Middle Road, No.277 Water Street, No.756 Tiantong South Road, Ningbo Zhejiang, China, 315199
- Owner or operator
- Ningbo Youhuan Automation Technology Co., Ltd. (10092336)
- Roles
- Manufacturer
- First device listed
- December 24, 2024
- Registered through
- 2026
- Brand names listed
- Power wheelchair, Power wheelchair: YH-E6011, YH-E6013A, Transfer Chair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Transfer, Patient, Manual | FMR | 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 |
|---|---|---|---|---|---|---|
| March 26, 2025 | K250134 | Power Wheelchair (YH-E6011,YH-E6013A) | ITI | Substantially Equivalent | Ningbo Youhuan Automation Technology Co., Ltd. | accessdata.fda.gov |
| September 16, 2024 | K240638 | Power Wheelchair (YH-E7007) | ITI | Substantially Equivalent | Ningbo Youhuan Automation Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 26, 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.