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Rexton, Inc.

United StatesFDA applicant, unverified

Devices
21

What Rexton, Inc. makes

Rexton, Inc. manufactures behind-the-ear hearing aids, including models like MICRO MINI PRIMO AGC, MINI PRIMO PLUS ASP, and REXTON RX12 POWER PLUS WITH DUAL RECEIVER. They also produce programmable instruments such as the ORION PPM, PP, PP-D, and the HORIZON FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMABLE INSTRUMENTS.

Rexton's devices are listed in the FDA 510(k) registry and are classified as Class I medical devices. The company is based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Rexton, Inc. have in the registry?

The registry currently lists 21 devices for Rexton, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rexton, Inc.'s devices?

Among its 21 most recently registered devices, Rexton, Inc. has devices listed in FDA 510(k) (21 devices).

What risk classes do Rexton, Inc.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Rexton, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Rexton, Inc. in the registry?

The most recently registered devices listed for Rexton, Inc. include MICRO MINI PRIMO AGC, MICRO-MINI PRIMO S-AGC, REXPLUS PP3, ORION PPM, PP, PP-D and REXTON RX12 POWER PLUS W/DUAL RECEIVER.

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