Lichtmega Technology Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lichtmega Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Lichtmega Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Sungo Management Consulting Company Limited. as regulatory consultant.
2 devices