Device recall
Z-2239-2009: ILUMAVision Software, version 2.1.0 Picture Archiving and Communication system…
FDA device recall · Class II · IMTEC IMAGING L.L.C.
Key facts
| Recall number (Z-number) | Z-2239-2009 |
|---|---|
| Recall event | 53132 |
| Product | ILUMAVision Software, version 2.1.0 Picture Archiving and Communication system Product used as a tool for the pre-surgical planning of the placement of dental implants and pre-surgical fabrication of stents to aid in dental implant insertion. In addition, it is used for diagnostics and treatment… |
| Product code | LLZ |
| Recalling firm | IMTEC IMAGING L.L.C. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 27, 2010 |
| 510(k) numbers | K081347 |
| FEI number | 1000118617 |
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