Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Magentiq Eye, Ltd. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K260724 | MAGENTIQ-COLO (ME-APDS) | Magentiq Eye, Ltd. | 2026-04-03 | 29 | 0 |
| K252178 | MAGENTIQ-COLO (ME-APDS) | Magentiq Eye, Ltd. | 2025-10-03 | 84 | 0 |
| K244023 | MAGENTIQ-COLO (ME-APDS) | Magentiq Eye, Ltd. | 2025-01-24 | 28 | 0 |
| K223473 | ME-APDS™; MAGENTIQ-COLO™ | Magentiq Eye, Ltd. | 2023-07-25 | 250 | 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