Hippoclinic
Country not established
- Devices
- 1
What Hippoclinic makes
Hippoclinic manufactures the HippoMind (v1.0), a medical device designed for cognitive assessment and monitoring in clinical settings.
The HippoMind (v1.0) is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
HippoMind (v1.0) Ref K251881
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hippoclinic have in the registry?
The registry currently lists 1 device for Hippoclinic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hippoclinic's devices?
Among its 1 most recently registered device, Hippoclinic has devices listed in FDA 510(k) (1 device).
What risk classes do Hippoclinic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hippoclinic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hippoclinic in the registry?
The most recently registered devices listed for Hippoclinic include HippoMind (v1.0).