Kinos Medical
Country not established
- Devices
- 1
What Kinos Medical makes
Kinos Medical manufactures the Kinos Axiom Total Ankle System, a prosthetic ankle replacement designed for patients requiring joint arthroplasty due to degenerative joint disease or trauma.
The company’s portfolio is regulated under FDA Class II devices, with the Kinos Axiom Total Ankle System authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Kinos Axiom Total Ankle System Ref K192778
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinos Medical have in the registry?
The registry currently lists 1 device for Kinos Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinos Medical's devices?
Among its 1 most recently registered device, Kinos Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Kinos Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kinos Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinos Medical in the registry?
The most recently registered devices listed for Kinos Medical include Kinos Axiom Total Ankle System.