510(k) K253657 · GDW Staple, Implantable
Tri-staple 2.0 Reloads; Endo GIA Reloads with Tri-Staple Technology; Endo GIA Gray Articulating Reloads; Signia Small Diameter Reloads
| Applicant | Covidien (Part of Medtronic), North Haven CT, US |
| Decision | Substantially Equivalent, Apr 10, 2026 |
| Received | Nov 20, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253657
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.