Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Velopex International, Inc. — 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) |
|---|---|---|---|---|---|
| K111167 | XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER | Velopex International, Inc. | 2011-08-18 | 114 | 0 |
| K093503 | INTRAX FILM PROCESSOR | Velopex International, Inc. | 2010-01-06 | 55 | 0 |
| K024105 | VELOPEX AQUACUT FLUID ABRASION UNIT | Velopex International, Inc. | 2003-10-09 | 300 | 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