Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
QEX · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K253407 | NeVa PV Thrombectomy Device | Vesalio, Inc. | 2025-11-24 | 55 | 0 |
| K171493 | MegaVac Mechanical Thrombectomy System | Capture Vascular, Inc. | 2017-08-10 | 80 | 0 |
| K163618 | INDIGO Aspiration System | Penumbra, Inc. | 2017-05-24 | 153 | 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