Device recall
Z-1186-2013: SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera…
FDA device recall · Class II · Discus Dental LLC
Key facts
| Recall number (Z-number) | Z-1186-2013 |
|---|---|
| Recall event | 64621 |
| Product | SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232. The SL3 is a soft-tissue diode laser intended to be used for dental procedures |
| Product code | GEX |
| Recalling firm | Discus Dental LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 29, 2013 |
| 510(k) numbers | K102639 |
| FEI number | 3002751089 |
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