Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Verticor, 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) |
|---|---|---|---|---|---|
| K110047 | VERTICOR K-WIRE SYSTEM | Verticor, Ltd. | 2011-02-28 | 53 | 0 |
| K103137 | VENUS ANTERIOR CERVICAL PLATE | Verticor, Ltd. | 2011-02-10 | 108 | 0 |
| K091426 | CERVICORE CORPECTOMY CAGE | Verticor, Ltd. | 2009-12-23 | 224 | 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