Device recall
Z-0543-05: Waterlase MD, dental laser unit, Model #6200218, serial numbers 10500210 to…
FDA device recall · Class III · Biolase Technology Inc
Key facts
| Recall number (Z-number) | Z-0543-05 |
|---|---|
| Recall event | 31106 |
| Product | Waterlase MD, dental laser unit, Model #6200218, serial numbers 10500210 to 105202680, inclusive. |
| Product code | LYB |
| Recalling firm | Biolase Technology Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 17, 2005 |
| 510(k) numbers | K031140 |
| FEI number | 2027755 |
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