Device recall
Z-0015-2022: Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression…
FDA device recall · Class II · Paltop Advanced Dental Solutions Ltd
Key facts
| Recall number (Z-number) | Z-0015-2022 |
|---|---|
| Recall event | 88576 |
| Product | Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative… |
| Product code | NDP |
| Recalling firm | Paltop Advanced Dental Solutions Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 21, 2023 |
| FEI number | 3009161350 |
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