Bellab
SwedenFDA applicant, unverified
- Devices
- 1
What Bellab makes
Bellab manufactures personal audio devices designed to improve hearing through air conduction amplification. These include assistive listening devices and personal amplifiers tailored for individual use.
The company’s products are regulated as Class II devices under FDA requirements, with authorisation supported through the 510(k) pathway. Bellab is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bellab have in the registry?
The registry currently lists 1 device for Bellab. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bellab's devices?
Among its 1 most recently registered device, Bellab has devices listed in FDA 510(k) (1 device).
What risk classes do Bellab's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bellab's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bellab in the registry?
The most recently registered devices listed for Bellab include AIR CONDUCTION ASSISTIVE LISTENING DEVICE.PERSONAL AMPLIFIER.