Data / Medical devices / China / Shenzhen Zuowei Technology Co.,ltd.
Shenzhen Zuowei Technology Co.,ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Zuowei Technology Co.,ltd. is registered with the FDA (registration 3023852281) in Shenzhen Guangdong, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 12, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023852281
- Address
- Floor 2nd, Bulding 7th, Yi Fenghua innovation industrial park, Dalang street, Xinshi Subdistrict, Longhua district, Shenzhen Guangdong, China, 518000
- Owner or operator
- SHENZHEN ZUOWEI TECHNOLOGY CO.,LTD. (10085647)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- July 13, 2022
- Registered through
- 2026
- Brand names listed
- Bed Shower Machine, Intelligent Incontinence Cleaning Robot, Smart Diaper Wetting Alarm Kit, Electric Lift Transfer Chair, Electric Toilet Raiser, Manual Lift Transfer Chair, Mechanical chair, Standup Wheelchair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Chair, Positioning, Electric | INO | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Patient Transfer, Powered | FRZ | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Transfer, Patient, Manual | FMR | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Standup | IPL | 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 12, 2025 | K243783 | Walking rehabilitation training electric wheelchair (ZW518) | IPL | Substantially Equivalent | Shenzhen Zuowei Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Positioning, Electric
- All makers of Chair, With Casters
- All makers of Device, Transfer, Patient, Manual
- All makers of Device, Patient Transfer, Powered
- All makers of Chair, Adjustable, Mechanical
- All makers of Wheelchair, Standup
Updated March 12, 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.