Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Wingderm Electro-Optics , Ltd. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K252599 | Diode Laser Therapy Systems (WLA-02) | Wingderm Electro-Optics , Ltd. | 2026-02-24 | 190 | 0 |
| K192350 | Medical Non-Ablative Fractional Laser Systems | Wingderm Electro-Optics , Ltd. | 2020-04-30 | 245 | 1 |
| K191611 | Diode Laser Therapy Systems | Wingderm Electro-Optics , Ltd. | 2019-07-31 | 44 | 1 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda