Clarimedex, Inc.
Country not established
- Devices
- 1
What Clarimedex, Inc. makes
Clarimedex, Inc. produces the MODEL 2200, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Model 2200 Ref K062635
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clarimedex, Inc. have in the registry?
The registry currently lists 1 device for Clarimedex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clarimedex, Inc.'s devices?
Among its 1 most recently registered device, Clarimedex, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Clarimedex, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Clarimedex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clarimedex, Inc. in the registry?
The most recently registered devices listed for Clarimedex, Inc. include MODEL 2200.