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Clinical Sciences, Inc.

United StatesFDA applicant, unverified

Devices
30

What Clinical Sciences, Inc. makes

Clinical Sciences, Inc. manufactures a range of diagnostic test kits and systems, including ELISA test kits for Varicella Zoster and CMV, as well as various immunoperoxidase and immunofluorescence kits for detecting antibodies such as antimitochondrial, antismooth muscle, and ANA. The company also produces specific viral antigen tests for Epstein-Barr virus, rapid plasma reagin card tests, and specialized culture media systems like the JEMBEC device.

The company is based in the United States, and its product portfolio consists of devices classified as Class I and Class II. These devices are listed within the FDA 510(k) regulatory registry.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

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

The registry currently lists 30 devices for Clinical Sciences, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clinical Sciences, Inc.'s devices?

Among its 30 most recently registered devices, Clinical Sciences, Inc. has devices listed in FDA 510(k) (30 devices).

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

Among its 30 most recently registered devices, the classes recorded for Clinical Sciences, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Clinical Sciences, Inc. include VARICELLA ZOSTER IGG CLIN-ELISA TEST KIT, IMMUNOP. ANTIMITOCHONDRIAL ANTIBODY KIT, EPSTEIN-BARR VIRAL CAPSID ANTIGEN IGG #4590 and EPSTEIN-BARR VIRUS (EBNA-1) IGG CATA. #4550.

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