Device recall
Z-0665-03: LTX Endosseous Implant 6.0 mm X 11.5 mm and also LTX Endosseous Implant 5.0 mm X…
FDA device recall · Class III · Implant Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-0665-03 |
|---|---|
| Recall event | 25722 |
| Product | LTX Endosseous Implant 6.0 mm X 11.5 mm and also LTX Endosseous Implant 5.0 mm X 15 mm, Sterile, |
| Product code | DZE |
| Recalling firm | Implant Innovations, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 3, 2012 |
| 510(k) numbers | K950204 |
| FEI number | 1038806 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database