Metavox, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Metavox, Inc. makes
Metavox, Inc. manufactures the MV-1000 Hearing Aid, a device designed for auditory amplification, and the MV-1000 Auditory Trainer, intended for speech and sound rehabilitation.
The company’s products are regulated under FDA’s 510(k) pathway, with the MV-1000 Hearing Aid classified as Class II and the MV-1000 Auditory Trainer as Class I. Both devices are listed in the FDA’s 510(k) database. Metavox, Inc. is based in the United States.
Catalogue
Metavox Mv-1000 Hearing Aid Ref K833152
Regimes: 510(k) Registry: 510(k)Metavox Mv-1000 Auditory Trainer Ref K832190
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metavox, Inc. have in the registry?
The registry currently lists 2 devices for Metavox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metavox, Inc.'s devices?
Among its 2 most recently registered devices, Metavox, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Metavox, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Metavox, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metavox, Inc. in the registry?
The most recently registered devices listed for Metavox, Inc. include METAVOX MV-1000 HEARING AID and METAVOX MV-1000 AUDITORY TRAINER.