Data / Medical devices / China / Shenzhen Sunsred Technology CO.,Ltd.
Shenzhen Sunsred Technology CO.,Ltd.: FDA-registered device maker in shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Sunsred Technology CO.,Ltd. is registered with the FDA (registration 3017382141) in shenzhen Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 20, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017382141
- Address
- 201, No. 22, Shijing Road, Fumin Community Fucheng Street, Longhua District Shenzhen, Guangdong, China, shenzhen Guangdong, China, 518110
- Owner or operator
- Shenzhen Sunsred Technology Co.,Ltd (10081443)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- June 26, 2025
- Registered through
- 2026
- Brand names listed
- LED Facial Mask,model:SR-M4
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 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 20, 2025 | K243978 | LED Facial Mask | OHS | Substantially Equivalent | Shenzhen Sunsred Technology Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Lamp, Infrared, Therapeutic Heating
Updated June 20, 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.