Device recall
Z-0231-2007: XiVE S plus Screw Implant D3.0/L13, Model Number 26-0123, Friadent GmbH. (dental…
FDA device recall · Class II · Dentsply Friadent Ceramed
Key facts
| Recall number (Z-number) | Z-0231-2007 |
|---|---|
| Recall event | 36844 |
| Product | XiVE S plus Screw Implant D3.0/L13, Model Number 26-0123, Friadent GmbH. (dental implant) |
| Product code | DZE |
| Recalling firm | Dentsply Friadent Ceramed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 30, 2007 |
| 510(k) numbers | K032750 |
| FEI number | 1721411 |
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