Dentimax
Country not established
- Devices
- 5
What Dentimax makes
Dentimax produces digital X-ray imaging systems, including sensors of sizes 1 and 2, and a USB control box for these devices.
The company's products are Class II medical devices listed in the FDA 510(k) registry, and Dentimax is based in the US.
Catalogue
- Registry: GUDID
- Registry: GUDID
OpenSensorX Series Ref K220556
Regimes: 510(k) Registry: 510(k)Digital X-Ray DentiMax Pro Imaging System Ref K251206
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentimax have in the registry?
The registry currently lists 5 devices for Dentimax. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentimax's devices?
Among its 5 most recently registered devices, Dentimax has devices listed in FDA 510(k) (3 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Dentimax's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dentimax's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dentimax in the registry?
The most recently registered devices listed for Dentimax include DentiMax Dream Sensor Size 2, DentiMax Dream Sensor Size 1, OpenSensorX Series and Digital X-Ray DentiMax Pro Imaging System.