Covidien, Formerly Valleylab,
Country not established
- Devices
- 1
What Covidien, Formerly Valleylab, makes
Covidien manufactures surgical sealing and dividing devices, including the LUGASURE system with curved, small-jaw, open-seal configurations designed for tissue division and coagulation in minimally invasive procedures.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via 510(k) clearance. Covidien is headquartered in the United States.
Catalogue
Lugasure Curved, Small Jaw, Open Sealer/Divider Ref K102470
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien, Formerly Valleylab, have in the registry?
The registry currently lists 1 device for Covidien, Formerly Valleylab,. Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien, Formerly Valleylab,'s devices?
Among its 1 most recently registered device, Covidien, Formerly Valleylab, has devices listed in FDA 510(k) (1 device).
What risk classes do Covidien, Formerly Valleylab,'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Covidien, Formerly Valleylab,'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien, Formerly Valleylab, in the registry?
The most recently registered devices listed for Covidien, Formerly Valleylab, include LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER.