Kineticor, Inc.
Country not established
- Devices
- 1
What Kineticor, Inc. makes
Kineticor, Inc. manufactures motion correction systems designed to stabilize imaging devices and reduce artifacts during medical procedures, ensuring clearer diagnostic results.
The company’s portfolio is classified under FDA’s Class II regulatory category and includes devices listed via the 510(k) clearance pathway. Kineticor operates from the United States.
Catalogue
Motion Correction System Ref K193324
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kineticor, Inc. have in the registry?
The registry currently lists 1 device for Kineticor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kineticor, Inc.'s devices?
Among its 1 most recently registered device, Kineticor, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kineticor, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kineticor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kineticor, Inc. in the registry?
The most recently registered devices listed for Kineticor, Inc. include Motion Correction System.