Eli Lilly and Company
Medical device manufacturer in Indianapolis, IL.
9510(k) clearances
0PMA approvals
1recalls
Device types
510(k) clearances
| 510(k) | Device | Decision |
|---|---|---|
| K212217 | Tempo Smart ButtonQOG · Traditional | 09/16/2022SE |
| K160949 | Go Dose SystemNDC · Traditional | 12/22/2016SE |
| K160668 | HumaPen SavvioFMF · Traditional | 06/03/2016SE |
| K151686 | HumanPen Ergo IIFMF · Traditional | 12/30/2015SE |
| K142518 | HumaPen LuxuraFMF · Traditional | 06/05/2015SE |
| K100988 | Humapen Luxura HDFMF · Traditional | 08/17/2010SE |
| K063151 | Humapen Luxura HDNSC · Traditional | 01/09/2007SE |
| K053563 | Humapen MemoirFMF · Traditional | 04/07/2006SE |
| K982842 | Humapen and Humapen ErgoFMF · Traditional | 09/25/1998SE |
Recalls
| Recall | Product | Initiated |
|---|---|---|
| Z-2191-2011 | Forteo [teriparatide (rDNA origin) injection] black starter kits containing Triad…Eli Lilly and Company announced 3/17/2011 that patients should not use the alcohol prep pads made by the… | 03/17/2011Terminated |