# Covidien, Formerly Valleylab,

- Location (FDA's records): Boulder, CO
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 5 (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
- Valleylab, Inc.: 2 (https://510kreport.com/company/valleylab)

## Firms that cite its devices most
- Covidien: 2 (https://510kreport.com/company/covidien)
- Covidien, Formerly Valleylab, A Division of Tyco H: 2 (https://510kreport.com/company/covidien-formerly-valleylab-a-division-of-tyco-h)
- Applied Medical Resources: 1 (https://510kreport.com/company/applied-medical-resources)

## Its most-cited devices
- K102470: Lugasure Curved, Small Jaw, Open Sealer/Divider (2011), cited by 5

## Recent decisions
- K102470: Lugasure Curved, Small Jaw, Open Sealer/Divider (Feb 7, 2011)

Source page: https://510kreport.com/company/covidien-formerly-valleylab