Dgi Technologies
Country not established
- Devices
- 2
What Dgi Technologies makes
Dgi Technologies manufactures the Claritag Advanced and Claritag, which are medical devices designed for continuous glucose monitoring (CGM) to track blood glucose levels in real time for diabetes management.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Claritag Advanced Ref K222356
Regimes: 510(k) Registry: 510(k)Claritag Ref K190747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dgi Technologies have in the registry?
The registry currently lists 2 devices for Dgi Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dgi Technologies's devices?
Among its 2 most recently registered devices, Dgi Technologies has devices listed in FDA 510(k) (2 devices).
What risk classes do Dgi Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dgi Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dgi Technologies in the registry?
The most recently registered devices listed for Dgi Technologies include Claritag Advanced and Claritag.