Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Duoject Medical Systems, 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) |
|---|---|---|---|---|---|
| K133097 | E-Z LINK | Duoject Medical Systems, Inc. | 2014-03-13 | 164 | 0 |
| K070584 | SMART-ROD | Duoject Medical Systems, Inc. | 2008-04-02 | 398 | 0 |
| K010703 | INTER-VIAL | Duoject Medical Systems, Inc. | 2001-06-25 | 108 | 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