Medical Device Manufacturer · US , Indianapolis , IN

Eli Lilly and Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Recent clearances: HUMAPEN LUXURA HD, HUMAPEN AND HUMAPEN ERGO

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Eli Lilly and Co. General Hospital ✕

2 devices

1-2 of 2

Cleared Jan 09, 2007

HUMAPEN LUXURA HD

General Hospital · 85d

Cleared Sep 25, 1998

HUMAPEN AND HUMAPEN ERGO

General Hospital · 44d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 09, 2026