Sommetrics
Country not established
- Devices
- 2
What Sommetrics makes
Sommetrics makes the cNEP Airway, a device used for monitoring respiratory function.
The cNEP Airway is a Class II medical device listed in the FDA 510(k) registry, and Sommetrics is based in the United States.
Catalogue
- Registry: GUDID
cNEP Airway Ref DEN140024
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Sommetrics have in the registry?
The registry currently lists 2 devices for Sommetrics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sommetrics's devices?
Among its 2 most recently registered devices, Sommetrics has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Sommetrics's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sommetrics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sommetrics in the registry?
The most recently registered devices listed for Sommetrics include aerFree Airway Management System (AMS) 30-5001 and cNEP Airway.