Device recall
Z-2162-2026: Diowave Laser System, REF: Diowave 250W
FDA device recall · Class II · Technological Medical Advancements LLC
Key facts
| Recall number (Z-number) | Z-2162-2026 |
|---|---|
| Recall event | 98507 |
| Product | Diowave Laser System, REF: Diowave 250W |
| Product code | ILY |
| Recalling firm | Technological Medical Advancements LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K121363 |
| FEI number | 3009346095 |
At a glance
- 1–9 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