# Surgical Devices, A Divsion of Tyco Healthcare

- Location (FDA's records): North Haven, CT
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: GDW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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 Lp, Formerly Registered AS United States: 1 (https://510kreport.com/company/covidien-lp-formerly-registered-as-united-states)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)

## Firms that cite its devices most
- Covidien, Formerly US Surgical A Divison of Tyco H: 2 (https://510kreport.com/company/covidien-formerly-us-surgical-a-divison-of-tyco-h)
- Covidien: 1 (https://510kreport.com/company/covidien)

## Its most-cited devices
- K093410: Autosuture Endo Gia Single Use Black Reload with Tri-Staple Technology (2009), cited by 3

## Recent decisions
- K093410: Autosuture Endo Gia Single Use Black Reload with Tri-Staple Technology (Nov 12, 2009)

Source page: https://510kreport.com/company/surgical-devices-a-divsion-of-tyco-healthcare