Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Weifang Mingliang Electronics Co., 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) |
|---|---|---|---|---|---|
| K260307 | Diode Laser Therapy Systems (V19) | Weifang Mingliang Electronics Co., Ltd. | 2026-04-15 | 75 | 0 |
| K242183 | Fractional CO2 Laser Therapy System (EXFU CO2) | Weifang Mingliang Electronics Co., Ltd. | 2024-10-23 | 90 | 0 |
| K200525 | Medical Diode Laser Hair Removal System | Weifang Mingliang Electronics Co., Ltd. | 2020-05-27 | 86 | 0 |
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