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Heine USA, Ltd.

Country not established

Devices
1

What Heine USA, Ltd. makes

Heine USA, Ltd. manufactures the HEINE LAMBDA 100, a device designed for precise measurement and analysis in laboratory settings, likely used for spectral analysis or light-based diagnostics.

The HEINE LAMBDA 100 is classified as a Class I medical device under FDA regulations and is listed via a 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

  • Heine Lambda 100 Ref K944156

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

Frequently asked questions

How many devices does Heine USA, Ltd. have in the registry?

The registry currently lists 1 device for Heine USA, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Heine USA, Ltd.'s devices?

Among its 1 most recently registered device, Heine USA, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Heine USA, Ltd.'s devices fall under?

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

What are the newest devices from Heine USA, Ltd. in the registry?

The most recently registered devices listed for Heine USA, Ltd. include HEINE LAMBDA 100.

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