Bose Corporation
United StatesFDA applicant, unverified
- Devices
- 23
What Bose Corporation makes
Bose Corporation manufactures rechargeable hearing aids designed to provide customizable sound control and amplification for users with hearing loss. These devices incorporate advanced audio technology to enhance speech clarity and reduce background noise, with features tailored for both mild and moderate hearing impairments.
The company’s hearing aid portfolio is classified as Class II under FDA regulations and is authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database and are intended for commercial distribution in the United States.
Catalogue
Search and filter all 23 devicesCompany details
- DUNS number
- 002579431
- [email protected]
- Phone
- 1-877-230-5639
Frequently asked questions
How many devices does BOSE CORPORATION have in the registry?
The registry currently lists 23 devices for BOSE CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list BOSE CORPORATION's devices?
Among its 23 most recently registered devices, BOSE CORPORATION has devices listed in FDA 510(k) (2 devices) and FDA GUDID (21 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do BOSE CORPORATION's devices fall under?
Among its 23 most recently registered devices, the classes recorded for BOSE CORPORATION's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BOSE CORPORATION in the registry?
The most recently registered devices listed for BOSE CORPORATION include Bose Frames BMD0005, Bose Hear App 865924-0010, Bose Frames BMD0004 and Bose Frames BMD0006.