Turtle Beach Corporation
Country not established
- Devices
- 2
Catalogue
- GUDID
HyperSound Tinnitus Module Ref K161331
510(k) 510(k)
Company details
- DUNS number
- 059286532
- [email protected]
- Phone
- 888-496-8001
Frequently asked questions
How many devices does Turtle Beach Corporation have in the registry?
The registry currently lists 2 devices for Turtle Beach Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Turtle Beach Corporation's devices?
Among its 2 most recently registered devices, Turtle Beach Corporation 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 Turtle Beach Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Turtle Beach Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Turtle Beach Corporation in the registry?
The most recently registered devices listed for Turtle Beach Corporation include HyperSound HyperSound Clear 500P and HyperSound Tinnitus Module.