# Covidien Lp, Formerly Know AS Valleylab, A Divison

- Location (FDA's records): Boulder, CO
- FDA decisions: 2 (2008–2011): 2 510(k) clearances
- Product codes: GEI (1), NEY (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 7 (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)
- Valleylab,A Division of Tyco Healthcare Group LP: 1 (https://510kreport.com/company/valleylab-a-division-of-tyco-healthcare-group)
- Erbe USA, Inc.: 1 (https://510kreport.com/company/erbe-usa)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Gyrus Acmi, Inc.: 1 (https://510kreport.com/company/gyrus-acmi)

## Firms that cite its devices most
- Covidien: 3 (https://510kreport.com/company/covidien)
- Neuwave Medical, Inc.: 1 (https://510kreport.com/company/neuwave-medical)
- Intuitive Surgical, Inc.: 1 (https://510kreport.com/company/intuitive-surgical)
- Acoustic Medsystems, Inc.: 1 (https://510kreport.com/company/acoustic-medsystems)
- Bsd Medical Corp.: 1 (https://510kreport.com/company/bsd-medical)

## Its most-cited devices
- K072687: Valleylab Microwave Ablation Generator (2008), cited by 4
- K110268: Forcetriad Electrosurgical Generator (2011), cited by 3

## Recent decisions
- K110268: Forcetriad Electrosurgical Generator (May 31, 2011)
- K072687: Valleylab Microwave Ablation Generator (Nov 25, 2008)

Source page: https://510kreport.com/company/covidien-lp-formerly-know-as-valleylab-a-divison