Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Heeyoung 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) |
|---|---|---|---|---|---|
| K073358 | LUMIMED SERIES 5MP DIGITAL FLAT PANEL DISPLAY SYSTEM, MODEL | Heeyoung Co., Ltd. | 2008-04-25 | 148 | 0 |
| K073292 | MM/MMA/COLOR SERIES DIGITAL FLAT PANEL DISPLAY SYSTEM | Heeyoung Co., Ltd. | 2008-01-18 | 56 | 0 |
| K052120 | LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 | Heeyoung Co., Ltd. | 2005-12-16 | 134 | 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