Device recall
Z-0417-2026: Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with…
FDA device recall · Class II · Prismatik Dentalcraft, Inc.
Key facts
| Recall number (Z-number) | Z-0417-2026 |
|---|---|
| Recall event | 97720 |
| Product | Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm Model/Catalog Number: 70-1047-COM0117 |
| Product code | NHA |
| Recalling firm | Prismatik Dentalcraft, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K142115 |
| FEI number | 3011649314 |
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