US Endo, Inc.
Country not established
- Devices
- 1
What US Endo, Inc. makes
Us Endo, Inc. manufactures monopolar electrodes and their associated cables, designed for use in medical procedures requiring controlled electrical stimulation or tissue ablation.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Monopolar Electrodes And Cables Ref K992485
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Us Endo, Inc. have in the registry?
The registry currently lists 1 device for Us Endo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Us Endo, Inc.'s devices?
Among its 1 most recently registered device, Us Endo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Us Endo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Us Endo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Us Endo, Inc. in the registry?
The most recently registered devices listed for Us Endo, Inc. include MONOPOLAR ELECTRODES AND CABLES.