Device recall
Z-0233-2023: GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02
FDA device recall · Class II · Sonendo Inc
Key facts
| Recall number (Z-number) | Z-0233-2023 |
|---|---|
| Recall event | 91045 |
| Product | GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02 |
| Product code | ELC |
| Recalling firm | Sonendo Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K190359 |
| FEI number | 3010817521 |
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