Data / Medical devices / China / Shenzhen Yattll Industry Co., Ltd
Shenzhen Yattll Industry Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Yattll Industry Co., Ltd is registered with the FDA (registration 3036988603) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 11, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036988603
- Address
- Room 907, A&I International Center, No. 8 Gaoerfu blvd, Longhua Dist, Shenzhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Yattll Industry Co., Ltd (10092742)
- Roles
- Manufacturer
- First device listed
- February 13, 2025
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair (YE200)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| January 11, 2025 | K241641 | Electric Wheelchair (YE200) | ITI | Substantially Equivalent | Shenzhen Yattll Industry Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 11, 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.