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Birch Point Medical, Inc.

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Devices
1

What Birch Point Medical, Inc. makes

Birch Point Medical, Inc. manufactures the IONTOPATCH, a transdermal iontophoresis device designed for localized drug delivery through the skin.

The IONTOPATCH is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Iontopatch Ref K992708 Open recall

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

Frequently asked questions

How many devices does Birch Point Medical, Inc. have in the registry?

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

Which registries list Birch Point Medical, Inc.'s devices?

Among its 1 most recently registered device, Birch Point Medical, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Birch Point Medical, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Birch Point Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Birch Point Medical, Inc. in the registry?

The most recently registered devices listed for Birch Point Medical, Inc. include IONTOPATCH.

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