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Sign in to claim this brandELI LILLY AND COMPANY
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- xxx.xxx
- —
- —
- [email protected]
- Phone
- 1-855-545-5983
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 006421325
Catalogue (32)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lilly Together | MA9161 Android (Version 15) | FDA UDI | Class I | Active |
| Lilly Together | MA9142 IOS (Version 17) | FDA UDI | Class I | Active |
| Tempo Welcome Kit | MS9841 | FDA UDI | Class II | Active |
| HumaPen® Luxura™ HD | MS9673 | FDA UDI | Class II | Active |
| Lilly Together | MA9158 IOS (Version 13) | FDA UDI | Class I | Active |
| ZYPREXA® Relprevv™ 300 mg Convenience Kit | VL7636 | FDA UDI | Class II | Active |
| Lilly Together | MA7723 IOS | FDA UDI | Class I | Active |
| Lilly Together | MA9140 IOS (Version 12) | FDA UDI | Class I | Active |
| ZYPREXA® Relprevv™ 405 mg Convenience Kit | VL7637 | FDA UDI | Class II | Active |
| HumatroPen® 12 mg | MS9561 | FDA UDI | Class II | Active |
| Lilly Together | MA9141 Android (Version 17) | FDA UDI | Class I | Active |
| ZYPREXA® Relprevv™ 210 mg Convenience Kit | VL7635 | FDA UDI | Class II | Active |
| Lilly Together | MA9131 Android | FDA UDI | Class I | Active |
| HumatroPen® 6 mg | MS9560 | FDA UDI | Class II | Active |
| Lilly Together | MA9160 IOS (Version 14) | FDA UDI | Class I | Active |
| Lilly Together | MA9135 ANDROID (Version 12) | FDA UDI | Class I | Active |
| HumaPen® Luxura™ HD - SAMPLE | MS9675 | FDA UDI | Class II | Active |
| Tempo Smart Button | MS6303 | FDA UDI | Class II | Active |
| Lilly Together | MA9162 IOS (Version 15) | FDA UDI | Class I | Active |
| Lilly Together | MA9152 Android (Version 13) | FDA UDI | Class I | Active |
| Tempo Refill Kit | MC0002 | FDA UDI | Class II | Active |
| Lilly Together | MA9159 Android (Version 14) | FDA UDI | Class I | Active |
| HumatroPen® 24 mg | MS9562 | FDA UDI | Class II | Active |
| Tempo Refill Kit | MS9599 | FDA UDI | Class II | Unknown |
| HumaPen Savvio | K160668 | FDA 510(k) | Class II | Active |
| HumanPen Ergo II | K151686 | FDA 510(k) | Class II | Active |
| Humapen And Humapen Ergo | K982842 | FDA 510(k) | Class II | Active |
| HumaPen Luxura | K142518 | FDA 510(k) | Class II | Active |
| Humapen Luxura Hd | K100988 | FDA 510(k) | Class II | Active |
| Go Dose System | K160949 | FDA 510(k) | Class II | Active |
| Humapen Luxura Hd | K063151 | FDA 510(k) | Class II | Active |
| Humapen Memoir | K053563 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 17, 2011 | Z-2191-2011 | — | terminated | Eli Lilly and Company announced 3/17/2011 that patients should not use the alcohol prep pads made by the Triad Group that are contained in the black starter kits for Forteo [teriparatide (rDNA origin) injection] in the United States.The Tri-ad Group is recalling the alcohol prep pads due to potential contamination with the bacteria, Ba-cillus cereus, which could result in life threatening infecti |