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Thermascan, Inc.

Country not established

Devices
1

What Thermascan, Inc. makes

Thermascan, Inc. manufactures the BREAST-SCAN™, a diagnostic device designed for breast imaging and screening.

The BREAST-SCAN™ is classified as a Class I medical device under FDA regulations and is 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

  • Breast-Scan(Tm) Ref K872962

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

Frequently asked questions

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

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

Which registries list Thermascan, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Thermascan, Inc. include BREAST-SCAN(TM).

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