# Covidien (Part of Medtronic)

- Location (FDA's records): North Haven, CT
- FDA decisions: 2 (2024–2026): 2 510(k) clearances
- Product codes: GDW (1), GAG (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Covidien: 3 (https://510kreport.com/company/covidien)
- Ethicon Endo-Surgery, Inc.: 2 (https://510kreport.com/company/ethicon-endo-surgery)
- Covidien, Formerly US Surgical A Divison of Tyco H: 1 (https://510kreport.com/company/covidien-formerly-us-surgical-a-divison-of-tyco-h)

## Recent decisions
- K253657: Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray Articulating Reloads; Signia™ Small Diameter Reloads (Apr 10, 2026)
- K240881: Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL) (Nov 1, 2024)

Source page: https://510kreport.com/company/covidien-part-of-medtronic