Class II — WINGDERM ELECTRO-OPTICS LTD.
| Recalling firm | Wingderm Electro-Optics Ltd. |
|---|---|
| Registered facility | WINGDERM ELECTRO-OPTICS LTD. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | All model WLA-01 systems sold to US customers are found to have labeling non-compliances |
| Product | Diode Laser Hair Removal model: WLA-01 |
| Distribution | Worldwide Distribution |
| Initiated | 2024-08-23 |
| Classified | 2024-12-05 |
| Recall number | Z-0556-2025 |
| Initiation | FDA Mandated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — WINGDERM ELECTRO-OPTICS LTD. (Z-0556-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95831/
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