Certis Health
Country not established
- Devices
- 1
What Certis Health makes
Certis Health manufactures the Presero 3D Scanning System, a device designed for three-dimensional imaging and scanning applications in medical settings.
The Presero 3D Scanning System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Presero 3D Scanning System Ref K190074
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Certis Health have in the registry?
The registry currently lists 1 device for Certis Health. Devices recorded under merged duplicate company entries are counted once.
Which registries list Certis Health's devices?
Among its 1 most recently registered device, Certis Health has devices listed in FDA 510(k) (1 device).
What risk classes do Certis Health's devices fall under?
Among its 1 most recently registered device, the classes recorded for Certis Health's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Certis Health in the registry?
The most recently registered devices listed for Certis Health include Presero 3D Scanning System.