Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Wingderm Electro-Optics with 3 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Feb 24, 2026: Diode Laser Therapy Systems (WLA-02).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 24, 2026 | Diode Laser Therapy Systems (WLA-02)K252599 · GEX | 510(k) clearances |
| Aug 23, 2024 | Non-ablative Fractional Laser Systems, Model: WFB-01Class II · Model WFB-01 sold to US customers before Aug 23, 2022 has been found to have a software bug (6 units). All WFB-01 models | Device recalls |
| Aug 23, 2024 | Diode Laser Hair Removal model: WLA-01Class II · All model WLA-01 systems sold to US customers are found to have labeling non-compliances | Device recalls |
| Apr 30, 2020 | Medical Non-Ablative Fractional Laser SystemsK192350 · ONG | 510(k) clearances |
| Jul 31, 2019 | Diode Laser Therapy SystemsK191611 · GEX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
