Device recall
Z-1592-2011: Straumann coDiagnostiX, dental implant planning system. Software Version 7.0…
FDA device recall · Class II · Straumann Manufacturing Inc.
Key facts
| Recall number (Z-number) | Z-1592-2011 |
|---|---|
| Recall event | 56994 |
| Product | Straumann coDiagnostiX, dental implant planning system. Software Version 7.0 including updates 7.0.2 and 7.0.2.10 |
| Product code | LLZ |
| Recalling firm | Straumann Manufacturing Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2011 |
| 510(k) numbers | K071636 |
| FEI number | 1000121052 |
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