Kinetix
Country not established
- Devices
- 4
What Kinetix makes
Kinetix manufactures respiratory devices including respirometers, inspiroeters, improved mouthpieces, and Kinetix mouthpieces.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Respirometer Ref K832401
Regimes: 510(k) Registry: 510(k)Inspirometer Ref K833012
Regimes: 510(k) Registry: 510(k)Improved Mouthpiece Ref K840459
Regimes: 510(k) Registry: 510(k)Kinetix Mouthpiece Ref K833420
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetix have in the registry?
The registry currently lists 4 devices for Kinetix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetix's devices?
Among its 4 most recently registered devices, Kinetix has devices listed in FDA 510(k) (4 devices).
What risk classes do Kinetix's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Kinetix's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetix in the registry?
The most recently registered devices listed for Kinetix include RESPIROMETER, INSPIROMETER, IMPROVED MOUTHPIECE and KINETIX MOUTHPIECE.