Device recall
Z-2263-2014: WaterLase iPlus Dental Laser System, Part No. 7200854-XX Software Upgrade Kit…
FDA device recall · Class II · Biolase Technology Inc
Key facts
| Recall number (Z-number) | Z-2263-2014 |
|---|---|
| Recall event | 68870 |
| Product | WaterLase iPlus Dental Laser System, Part No. 7200854-XX Software Upgrade Kit, Part No. 6201463. |
| Product code | GEX |
| Recalling firm | Biolase Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2014 |
| 510(k) numbers | K101658 |
| FEI number | 2027755 |
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