Igi Technologies
Country not established
- Devices
- 1
What Igi Technologies makes
Igi Technologies manufactures the IGTFusion device, 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
IGTFusion Ref K180522
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Igi Technologies have in the registry?
The registry currently lists 1 device for Igi Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Igi Technologies's devices?
Among its 1 most recently registered device, Igi Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Igi Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Igi Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Igi Technologies in the registry?
The most recently registered devices listed for Igi Technologies include IGTFusion.