Data / Medical devices / China / Shenzhen Century Dongyuan Technology Co. Ltd
Shenzhen Century Dongyuan Technology Co. Ltd: FDA-registered device maker in SHENZHEN Guangdong, China, 1 510(k) clearance
Shenzhen Century Dongyuan Technology Co. Ltd is registered with the FDA (registration 3021329660) in SHENZHEN Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 12, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021329660
- Address
- Floor 2, Building B1, Gonghe Fourth Industrial Zone, Shajing Street, Bao 'an District, Shenzhen City, SHENZHEN Guangdong, China, 518104
- Owner or operator
- Shenzhen Century Dongyuan Technology Co. LTD (10083490)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 24, 2021
- Registered through
- 2026
- Brand names listed
- Device, medical examination, ac powered, IPL Hair Removal Device, AI01, AI06, AI08, Al16, Al17, AI08, AI09, Light based over-the-counter hair removal
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Medical Examination, Ac Powered | KZF | 1 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| August 12, 2022 | K221466 | IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17 | OHT | Substantially Equivalent | Shenzhen Century Dongyuan Technology CO , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Medical Examination, Ac Powered
- All makers of Light Based Over-The-Counter Hair Removal
Updated August 12, 2022. 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.