Aze, Ltd.
Country not established
- Devices
- 3
What Aze, Ltd. makes
Aze, Ltd. develops medical imaging software for analyzing and processing MRI data, including tools for virtual place reconstruction and flow analysis, as well as specialized software for cardiac imaging and diagnostic support.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance pathway. Its portfolio is regulated in the United States.
Catalogue
Aze Virtualplace-Mr Flow Analysis Software Ref K102534
510(k) 510(k)Aze Virtualplace Ref K060453
510(k) 510(k)Aze Phoenix Software Ref K133521
510(k) 510(k)
Frequently asked questions
How many devices does Aze, Ltd. have in the registry?
The registry currently lists 3 devices for Aze, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aze, Ltd.'s devices?
Among its 3 most recently registered devices, Aze, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Aze, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Aze, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aze, Ltd. in the registry?
The most recently registered devices listed for Aze, Ltd. include AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE, AZE VIRTUALPLACE and AZE PHOENIX SOFTWARE.