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Mauch Laboratories, Inc.

Country not established

Devices
1

What Mauch Laboratories, Inc. makes

Mauch Laboratories, Inc. manufactures external ankle and foot orthotic devices designed to support or correct foot and ankle alignment.

These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Ankle/Foot External Ref K820505

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

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

The registry currently lists 1 device for Mauch Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mauch Laboratories, Inc.'s devices?

Among its 1 most recently registered device, Mauch Laboratories, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Mauch Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Mauch Laboratories, Inc. include ANKLE/FOOT EXTERNAL.

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