Shanghai Omni Laser Skinology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shanghai Omni Laser Skinology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Phototherapy System (OL-PDT950), Diode Laser Hair Removal System (RD-SLD600), Painless IPL System - KDT750
3
Total
3
Cleared
0
Denied
Shanghai Omni Laser Skinology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shanghai Omni Laser Skinology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by New Risen Enterprise Management Consulting Co.,Ltd as regulatory consultant.
FDA 510(k) Regulatory Record - Shanghai Omni Laser Skinology Co., Ltd.
3 devices