Slinph Technologies Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Slinph Technologies Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: iHelmet Laser Comb, iHelmet Hair Growth System
3
Total
3
Cleared
0
Denied
Slinph Technologies Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Slinph Technologies Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Sk Medical Device International Corp. and Guangzhou GLOMED Biological Technology Co., Ltd..
FDA 510(k) Regulatory Record - Slinph Technologies Co., Ltd.
3 devices