Usifroid
Country not established
- Devices
- 1
What Usifroid makes
Usifroid manufactures a flexible linear reducer designed for mitral and tricuspid valve procedures, intended to facilitate precise mechanical adjustment during surgical interventions.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via the 510(k) pathway. Usifroid operates from the United States.
Catalogue
Flexible Linear Reducer F/Mitral & Tric. Ref K800147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Usifroid have in the registry?
The registry currently lists 1 device for Usifroid. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usifroid's devices?
Among its 1 most recently registered device, Usifroid has devices listed in FDA 510(k) (1 device).
What risk classes do Usifroid's devices fall under?
Among its 1 most recently registered device, the classes recorded for Usifroid's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usifroid in the registry?
The most recently registered devices listed for Usifroid include FLEXIBLE LINEAR REDUCER F/MITRAL & TRIC..