SZ KKS Silicone&Electronic Co., Ltd. - FDA 510(k) Cleared Devices
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.
1 devices