Device recall
Z-0780-2016: IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product…
FDA device recall · Class II · Zimmer Dental Inc
Key facts
| Recall number (Z-number) | Z-0780-2016 |
|---|---|
| Recall event | 73013 |
| Product | IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more missing teeth… |
| Product code | DZE |
| Recalling firm | Zimmer Dental Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2016 |
| 510(k) numbers | K112160 |
| FEI number | 1038806 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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