Suunto USA
Country not established
- Devices
- 1
What Suunto USA makes
Suunto USA manufactures Class I medical devices, including the CEBE 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
Cebe Ref K971644
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Suunto USA have in the registry?
The registry currently lists 1 device for Suunto USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suunto USA's devices?
Among its 1 most recently registered device, Suunto USA has devices listed in FDA 510(k) (1 device).
What risk classes do Suunto USA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Suunto USA's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Suunto USA in the registry?
The most recently registered devices listed for Suunto USA include CEBE.