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Clinical Convenience Products, Inc.

United StatesFDA applicant, unverified

Devices
6

What Clinical Convenience Products, Inc. makes

Clinical Convenience Products, Inc. manufactures microbiological culture systems for clinical diagnostics, including MacConkey, Columbia CNA, and Modified TSA agar plates, as well as specialized systems like CLED and EMB media for bacterial isolation and identification.

These products are classified as Class I medical devices under FDA regulations and are 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.

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

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

The registry currently lists 6 devices for Clinical Convenience Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clinical Convenience Products, Inc.'s devices?

Among its 6 most recently registered devices, Clinical Convenience Products, Inc. has devices listed in FDA 510(k) (6 devices).

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

Among its 6 most recently registered devices, the classes recorded for Clinical Convenience Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Clinical Convenience Products, Inc. include CULTURIA MACCONKEY/COLUMBIA CNA, CULTURIA MACCONKEY/CLED #DM87, CULTURIA EMB/COLUMBIA CNA W/5% SHEEP and CULTURIA MACCONKEY-MUG/CLED SYSTEMS.

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