Data / Medical devices / China / SZ KKS Silicone&electronic Co., Ltd.
SZ KKS Silicone&electronic Co., Ltd.: FDA-registered device maker in SHENZHEN Guangdong, China, 1 510(k) clearance
SZ KKS Silicone&electronic Co., Ltd. is registered with the FDA (registration 3026890286) in SHENZHEN Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026890286
- Address
- 1ST, 2ND, 3RD, And 4TH Floors, No. 5 Baisha Road Xinqiao Community, Xinqiao Subdistrict, Bao'an District, SHENZHEN Guangdong, China, 518100
- Owner or operator
- SZ KKS Silicone&Electronic Co., Ltd. (10095438)
- Roles
- Manufacturer
- First device listed
- March 12, 2026
- Registered through
- 2026
- Brand names listed
- LED Light Therapy Silicone Face Mask(Model:kks-225, kks-280, kks-281), Panther II- LED Skin Rejuvenate Face, Neck and Decollete Mask(Prospera, model:DL035A)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 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 |
|---|---|---|---|---|---|---|
| February 12, 2026 | K254007 | LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281) | OHS | Substantially Equivalent | SZ KKS Silicone&Electronic Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Over-The-Counter Powered Light Based Laser For Acne
Updated February 12, 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.