# Surgical Devices, A Global Business Unit Covidien

- Location (FDA's records): North Haven, CT
- FDA decisions: 3 (2008–2009): 3 510(k) clearances
- Product codes: GAT (2), GDW (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Davis & Geck, Inc.: 1 (https://510kreport.com/company/davis-geck)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)

## Recent decisions
- K091016: Covidien Sports Surgery as Meniscal Repair Device with High Strength Suture (May 4, 2009)
- K083781: Eea Hemorrhoid Stapler & Accessories (Feb 4, 2009)
- K082535: Covidien Sports Surgery as Meniscal Repair Device (Dec 1, 2008)

Source page: https://510kreport.com/company/surgical-devices-a-global-business-unit-covidien