Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medpro Safety Products, 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) |
|---|---|---|---|---|---|
| K111424 | VACUETTE PREMIUM SAFETY NEEDLE SYSTEM TUBE-TOUCH | Medpro Safety Products, Inc. | 2011-07-29 | 67 | 0 |
| K102010 | VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET | Medpro Safety Products, Inc. | 2010-11-19 | 126 | 0 |
| K072602 | VACUETTE PREMIUM SAFETY NEEDLE SYSTEM | Medpro Safety Products, Inc. | 2008-06-18 | 278 | 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