Medical Device Manufacturer · US , Indianapolis , IN

Eli Lilly and Company - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

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) cleared devices by Eli Lilly and Company

5 devices

1-5 of 5