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Resound Corp.

United StatesFDA applicant, unverified

Devices
41

What Resound Corp. makes

Resound Corp. manufactures a range of rechargeable and non-rechargeable personal hearing aids, including models with Bluetooth connectivity, remote control options, and prescriptive programming systems. Their portfolio includes in-the-canal (ITC) hearing enhancement systems, digital programmers, and standalone hearing solutions designed for customised auditory support. Some devices feature direct audio input (DAI) capabilities for improved sound transmission.

The company’s devices are classified under FDA categories Class I and Class II, with most submissions recorded in the FDA’s 510(k) registry. Products are listed in the United States, where regulatory compliance follows FDA requirements for hearing aids. No additional international registries are specified.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Resound Corp. have in the registry?

The registry currently lists 41 devices for Resound Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Resound Corp.'s devices?

Among its 41 most recently registered devices, Resound Corp. has devices listed in FDA 510(k) (41 devices).

What risk classes do Resound Corp.'s devices fall under?

Among its 41 most recently registered devices, the classes recorded for Resound Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Resound Corp. in the registry?

The most recently registered devices listed for Resound Corp. include HEARING AID - AIR CONDUCTION, RESOUND(R) PERSONAL HEARING SYSTEM ED-3 ENCORE, RESOUND PERSONAL HEARING SYSTEMS MODIFICATION and RESOUND PERSONAL HEARING SYSTEM ED3/S-E.

Generated automatically from registry data and not verified by a human reviewer.