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Vitrotec Laboratories, Inc.

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Devices
1

What Vitrotec Laboratories, Inc. makes

Vitrotec Laboratories, Inc. makes medical devices such as the TANGENT SYSTEM(TM) ANA PROFILE TEST KIT, which is a type of test kit.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Frequently asked questions

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

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

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

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

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

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

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

The most recently registered devices listed for Vitrotec Laboratories, Inc. include TANGENT SYSTEM(TM) ANA PROFILE TEST KIT.

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