Lexi Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lexi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ZedView
2
Total
2
Cleared
0
Denied
Lexi Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Last cleared in 2021. Active since 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Lexi Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lexi Co., Ltd.
2 devices