Eli Lilly and Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eli Lilly and Company - FDA 510(k) Cleared Devices
Recent clearances: Tempo Smart Button
5
Total
5
Cleared
0
Denied
Eli Lilly and Company has 5 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Last cleared in 2022. Active since 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Eli Lilly and Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eli Lilly and Company
5 devices