Kenneth Hilsen
Country not established
- Devices
- 1
What Kenneth Hilsen makes
Kenneth Hilsen manufactures snoring control devices designed to reduce or mitigate snoring symptoms in patients.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance and are listed in the US regulatory registry.
Catalogue
Snoring Control Device Ref K963591
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kenneth Hilsen have in the registry?
The registry currently lists 1 device for Kenneth Hilsen. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kenneth Hilsen's devices?
Among its 1 most recently registered device, Kenneth Hilsen has devices listed in FDA 510(k) (1 device).
What risk classes do Kenneth Hilsen's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kenneth Hilsen's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kenneth Hilsen in the registry?
The most recently registered devices listed for Kenneth Hilsen include SNORING CONTROL DEVICE.