Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Valeris Medical · 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) |
|---|---|---|---|---|---|
| K192810 | Apollo Suture Anchor System | Valeris Medical | 2020-03-11 | 162 | 0 |
| K152255 | BoneCam Suture Anchors | Valeris Medical | 2015-11-16 | 98 | 0 |
| K142230 | Apollo Suture Anchor System and Titan Screws | Valeris Medical | 2014-09-10 | 28 | 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