Ai Medic, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Ai Medic, Inc. makes
Ai Medic, Inc. develops AutoSeg, a software-as-a-medical-device (SaMD) designed for automated segmentation of medical imaging data, such as CT or MRI scans, to assist in diagnostic and treatment planning workflows.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
AutoSeg Ref K220039
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ai Medic, Inc. have in the registry?
The registry currently lists 1 device for Ai Medic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ai Medic, Inc.'s devices?
Among its 1 most recently registered device, Ai Medic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ai Medic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ai Medic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ai Medic, Inc. in the registry?
The most recently registered devices listed for Ai Medic, Inc. include AutoSeg.