SZ KKS Silicone&Electronic Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
SZ KKS Silicone&Electronic Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)
1
Total
1
Cleared
0
Denied
SZ KKS Silicone&Electronic Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by SZ KKS Silicone&Electronic Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guangzhou GLOMED Biological Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - SZ KKS Silicone&Electronic Co., Ltd.
1 devices