Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vectec — 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) |
|---|---|---|---|---|---|
| K121370 | VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE | Vectec | 2013-08-02 | 452 | 0 |
| K103707 | VECTEC DISPOSABLE MONOPOLAR CONNECTOR CABLE | Vectec | 2011-02-04 | 46 | 0 |
| K071976 | VECTEC DISPOSABLE TROCARS AND LAPAROSCOPIC ACCESSORIES | Vectec | 2007-09-06 | 51 | 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