Device recall
Z-0935-2014: LOCATOR Implant Attachment System. The LOCATOR Implant Attachment System is a…
FDA device recall · Class II · Zest Anchors LLC
Key facts
| Recall number (Z-number) | Z-0935-2014 |
|---|---|
| Recall event | 67315 |
| Product | LOCATOR Implant Attachment System. The LOCATOR Implant Attachment System is a universal hinge, resilient attachment for endosseous implants. The LOCATOR Implant Attachment System is designed for use with overdentures or partial dentures, retained in whole or in part, by endosseous implants in the… |
| Product code | DZE |
| Recalling firm | Zest Anchors LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2014 |
| 510(k) numbers | K072878, K994257 |
| FEI number | 2023950 |
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