Danavox, Inc.
United StatesFDA applicant, unverified
- Devices
- 26
What Danavox, Inc. makes
Danavox, Inc. manufactures a range of hearing aids, including in-the-ear, behind-the-ear, and body-worn models. Their portfolio includes custom-fit devices like the In-The-Ear Model 101M and Perceptor, as well as behind-the-ear options such as the Model 775, Series 123, and masking amplifiers like the 735S. Additional variants include the Hearing Aid Model 781, 787PP, and specialized behind-the-ear models like the 793U, M, UH, and MH.
The company’s devices are classified under FDA categories Class I and Class II, with regulatory records supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database. Danavox, Inc. is based in the United States.
Catalogue
Search and filter all 26 devicesFrequently asked questions
How many devices does Danavox, Inc. have in the registry?
The registry currently lists 26 devices for Danavox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Danavox, Inc.'s devices?
Among its 26 most recently registered devices, Danavox, Inc. has devices listed in FDA 510(k) (26 devices).
What risk classes do Danavox, Inc.'s devices fall under?
Among its 26 most recently registered devices, the classes recorded for Danavox, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Danavox, Inc. in the registry?
The most recently registered devices listed for Danavox, Inc. include HEARING AID, MODEL 781, IN-THE-EAR MODEL 101M, BEHIND-THE-EAR #123 AGCI and BEHIND-THE-EAR MODEL 115.