Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Lucero Medical, LLC — 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) |
|---|---|---|---|---|---|
| K200549 | Lucero Medical Cervical Cage System | Lucero Medical, LLC | 2020-12-16 | 288 | 0 |
| K122622 | ENDURAMESH | Lucero Medical, LLC | 2012-09-19 | 22 | 0 |
| K093207 | ENDURAMESH, MODEL 762.XXX | Lucero Medical, LLC | 2010-04-26 | 195 | 1 |
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