Lichtmega Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Lichtmega Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Scooter (PS30), Manual Wheelchair
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.
FDA 510(k) Regulatory Record - Lichtmega Technology Co., Ltd.
2 devices