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Maico Hearing Instruments, Inc.

United StatesFDA applicant, unverified

Devices
58

What Maico Hearing Instruments, Inc. makes

Maico Hearing Instruments, Inc. manufactures custom and non-custom hearing aids, including in-the-ear and behind-the-ear models with features like push-pull input compression. Their portfolio also includes audiometers for hearing assessments, such as the MA800 and MA610 impedance audiometers, as well as an aural acoustic screener for preliminary hearing evaluations.

The company’s devices are regulated under FDA Class I and Class II classifications, with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Maico Hearing Instruments, Inc. have in the registry?

The registry currently lists 58 devices for Maico Hearing Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Maico Hearing Instruments, Inc.'s devices?

Among its 50 most recently registered devices, Maico Hearing Instruments, Inc. has devices listed in FDA 510(k) (50 devices).

What risk classes do Maico Hearing Instruments, Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Maico Hearing Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Maico Hearing Instruments, Inc. in the registry?

The most recently registered devices listed for Maico Hearing Instruments, Inc. include FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR, HEARING AID, SERIES R, SERIES M PUSH-PULL INPUT COMPRESSION and MODEL P20/P21 IN-THE-EAR HEARING AID.

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