Covidien (Part of Medtronic)
Country not established
- Devices
- 2
What Covidien (Part of Medtronic) makes
The company manufactures surgical stapling and cutting devices, including reloads for linear and circular staplers. These include stapling reloads with articulating and small-diameter designs, as well as circular stapler adapters in standard and extended lengths.
The portfolio consists of Class II medical devices, authorised via FDA 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL) Ref K240881
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien (Part of Medtronic) have in the registry?
The registry currently lists 2 devices for Covidien (Part of Medtronic). Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien (Part of Medtronic)'s devices?
Among its 2 most recently registered devices, Covidien (Part of Medtronic) has devices listed in FDA 510(k) (2 devices).
What risk classes do Covidien (Part of Medtronic)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Covidien (Part of Medtronic)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien (Part of Medtronic) in the registry?
The most recently registered devices listed for Covidien (Part of Medtronic) include Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray Articulating Reloads; Signia™ Small Diameter Reloads and Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL).