Device recall
Z-1145-2014: Denlase: Diode Laser Therapy System and Penlase: Dental Laser Therapy System…
FDA device recall · Class II · China Daheng Group Inc.
Key facts
| Recall number (Z-number) | Z-1145-2014 |
|---|---|
| Recall event | 67520 |
| Product | Denlase: Diode Laser Therapy System and Penlase: Dental Laser Therapy System surgical powered. Surgical powered Laser instruments. |
| Product code | LYB |
| Recalling firm | China Daheng Group Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2015 |
| FEI number | 3008705657 |
At a glance
- None 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