Device recall
Z-0743-2025: Clarity Precision Grip Attachments, for use in orthodontic treatment. Part…
FDA device recall · Class II · 3M Company - Health Care Business
Key facts
| Recall number (Z-number) | Z-0743-2025 |
|---|---|
| Recall event | 95828 |
| Product | Clarity Precision Grip Attachments, for use in orthodontic treatment. Part numbers/SKUs: 359-830 359-831 359-832 359-833 359-834 359-835 359-836 359-837 |
| Product code | NXC |
| Recalling firm | 3M Company - Health Care Business |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K233257 |
| FEI number | 2110898 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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