Wingderm Electro-Optics , Ltd.
Wingderm Electro-Optics , Ltd. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2026, with 2 FDA device recalls on record.
Top product codes for Wingderm Electro-Optics , Ltd.
FDA recalls by Wingderm Electro-Optics , Ltd.
- Z-0555-2025 — Non-ablative Fractional Laser Systems, Model: WFB-01
- Z-0556-2025 — Diode Laser Hair Removal model: WLA-01
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Wingderm Electro-Optics , Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.