Device recall
Z-2204-2013: C2244.3820;, CONELOG Titanium Base CC 3.8GH2.0 inkl HS Product Usage: Endosseous…
FDA device recall · Class II · Camlog Usa
Key facts
| Recall number (Z-number) | Z-2204-2013 |
|---|---|
| Recall event | 66143 |
| Product | C2244.3820;, CONELOG Titanium Base CC 3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch. |
| Product code | NHA |
| Recalling firm | Camlog Usa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2014 |
| FEI number | 3004433109 |
At a glance
- None 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