Medqia
Country not established
- Devices
- 1
What Medqia makes
Medqia develops the IBIS EXPLORER software, a tool designed for image analysis and annotation in medical imaging workflows, enabling radiologists and clinicians to mark and review diagnostic images.
The IBIS EXPLORER software is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Ibis Explorer And Markup Software Ref K111319
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medqia have in the registry?
The registry currently lists 1 device for Medqia. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medqia's devices?
Among its 1 most recently registered device, Medqia has devices listed in FDA 510(k) (1 device).
What risk classes do Medqia's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medqia's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medqia in the registry?
The most recently registered devices listed for Medqia include IBIS EXPLORER AND MARKUP SOFTWARE.