Snorex (Nz), Ltd.
Country not established
- Devices
- 1
What Snorex (Nz), Ltd. makes
Snorex (NZ) Ltd. manufactures the SNOREX device, a medical solution designed to reduce snoring by creating a gentle airflow that opens the airway during sleep.
The SNOREX device is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Snorex Ref K971818
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Snorex (Nz), Ltd. have in the registry?
The registry currently lists 1 device for Snorex (Nz), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Snorex (Nz), Ltd.'s devices?
Among its 1 most recently registered device, Snorex (Nz), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Snorex (Nz), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Snorex (Nz), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Snorex (Nz), Ltd. in the registry?
The most recently registered devices listed for Snorex (Nz), Ltd. include SNOREX.