Data / Medical devices / China / Yurob Rehabilitation Medical Co.,ltd
Yurob Rehabilitation Medical Co.,ltd: FDA-registered device maker in Kunshan City Jiangsu, China, 4 510(k) clearances
Yurob Rehabilitation Medical Co.,ltd is registered with the FDA (registration 3030226288) in Kunshan City Jiangsu, China. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030226288
- Address
- No.93 Dianxing Road, Dianshanhu Town, Kunshan City Jiangsu, China, 215300
- Owner or operator
- Yurob Rehabilitation Medical Co.,Ltd (10089249)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 20, 2023
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair, Electric Wheelchair (HP206), Electrically Powered Wheelchair (YC-01), Electrically Powered Wheelchair (YM-01, YM-02), Scooter (YD-03)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| 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 3, 2026 | K253600 | Scooter (YD-03) | INI | Substantially Equivalent | Yurob Rehabilitation Medical Co., Ltd. | accessdata.fda.gov |
| March 27, 2026 | K253980 | Electrically Powered Wheelchair (Model YC-01) | ITI | Substantially Equivalent | Yurob Rehabilitation Medical Co., Ltd. | accessdata.fda.gov |
| February 12, 2025 | K243961 | Electrically Powered Wheelchair | ITI | Substantially Equivalent | Kunshan Hi-Fortune Health Products Co., Ltd. | accessdata.fda.gov |
| September 22, 2023 | K232193 | Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) | ITI | Substantially Equivalent | Yurob Rehabilitation Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 3, 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.