Mdai, Inc.
Country not established
- Devices
- 1
What Mdai, Inc. makes
Mdai, Inc. develops the MD.ai Viewer, a software tool designed for medical image analysis and interpretation, enabling healthcare providers to review and assess diagnostic imaging data.
The company’s portfolio is regulated under FDA’s Class II device classification, with individual products authorised through the 510(k) clearance pathway. The company is based in the United States.
Catalogue
MD.ai Viewer Ref K223425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mdai, Inc. have in the registry?
The registry currently lists 1 device for Mdai, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mdai, Inc.'s devices?
Among its 1 most recently registered device, Mdai, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mdai, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mdai, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mdai, Inc. in the registry?
The most recently registered devices listed for Mdai, Inc. include MD.ai Viewer.