SZ KKS Silicone&Electronic Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3026890286
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What SZ KKS Silicone&Electronic Co., Ltd. makes
SZ KKS Silicone&Electronic Co., Ltd. manufactures LED light therapy silicone face masks, including models kks-225, kks-280, and kks-281.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026890286
- DUNS number
- 546984470
- Address
- 1ST, 2ND, 3RD, AND 4TH FLOORS, NO. 5 BAISHA ROAD, SHENZHEN Guangdong
Frequently asked questions
How many devices does SZ KKS Silicone&Electronic Co., Ltd. have in the registry?
The registry currently lists 4 devices for SZ KKS Silicone&Electronic Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SZ KKS Silicone&Electronic Co., Ltd.'s devices?
Among its 4 most recently registered devices, SZ KKS Silicone&Electronic Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SZ KKS Silicone&Electronic Co., Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for SZ KKS Silicone&Electronic Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SZ KKS Silicone&Electronic Co., Ltd. in the registry?
The most recently registered devices listed for SZ KKS Silicone&Electronic Co., Ltd. include Kakusan kks-225, Kakusan kks-280, Kakusan kks-281 and LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281).