Device recall
Z-0505-2009: Sinu-Lift(TM) System, LLC., Model SLS-1, Sterile, Innovative Implant Technology…
FDA device recall · Class II · Innovative Implant Technology
Key facts
| Recall number (Z-number) | Z-0505-2009 |
|---|---|
| Recall event | 50168 |
| Product | Sinu-Lift(TM) System, LLC., Model SLS-1, Sterile, Innovative Implant Technology, The Sinu-Lift(TM) System is intended to : - Facilitate access to the maxillary sinus, - Lift the sinus membrane from the alveolar ridge of the maxilla with a minimum height of 5mm, and - Augment the space created by… |
| Product code | NDP |
| Recalling firm | Innovative Implant Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2009 |
| FEI number | 3006005748 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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