Fidelty Hearing Instruments, Inc.
Country not established
- Devices
- 1
What Fidelty Hearing Instruments, Inc. makes
Fidelty Hearing Instruments, Inc. manufactures the DOCE All-in-the-Ear hearing aid, a custom-fitted device designed for in-the-ear amplification of sound.
The company’s portfolio is regulated under FDA Class I devices and listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Doce All-In-The-Ear Aid Ref K822817
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fidelty Hearing Instruments, Inc. have in the registry?
The registry currently lists 1 device for Fidelty Hearing Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fidelty Hearing Instruments, Inc.'s devices?
Among its 1 most recently registered device, Fidelty Hearing Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fidelty Hearing Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fidelty Hearing Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fidelty Hearing Instruments, Inc. in the registry?
The most recently registered devices listed for Fidelty Hearing Instruments, Inc. include DOCE ALL-IN-THE-EAR AID.