Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Covidien (Part of Medtronic) · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K253657 | Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ | Covidien (Part of Medtronic) | 2026-04-10 | 141 | 0 |
| K240881 | Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Sig | Covidien (Part of Medtronic) | 2024-11-01 | 214 | 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