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Preferred Micro-Media

FDA registration: United States Last updated 23 May 2026

Devices
28
Registries
FDA 510(k)
FDA recalls
0

Catalogue28

What Preferred Micro-Media makes

Preferred Micro-Media manufactures microbiological culture media, including selective and differential agar plates and broths for identifying and isolating bacteria. Products include Tryptic Soy Agar with 5% Sheep Blood, MacConkey Agar, Chocolate Agar, and SIM Medium, among others. These media support bacterial growth and differentiation in clinical and laboratory settings.

The company’s portfolio is regulated under FDA’s Class I and Class II device classifications, with select products listed via the 510(k) pathway. These media are intended for in vitro diagnostic use and are tracked in the FDA’s regulatory database. Preferred Micro-Media operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

How many devices does Preferred Micro-Media have in the registry?

The registry currently lists 28 devices for Preferred Micro-Media. Devices recorded under merged duplicate company entries are counted once.

Which registries list Preferred Micro-Media's devices?

Among its 28 most recently registered devices, Preferred Micro-Media has devices listed in FDA 510(k) (28 devices).

What risk classes do Preferred Micro-Media's devices fall under?

Among its 28 most recently registered devices, the classes recorded for Preferred Micro-Media's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Preferred Micro-Media in the registry?

The most recently registered devices listed for Preferred Micro-Media include COLUMBIZ CNA AGAR W/5% SHEEP BLOOD, MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE, THAYER MARTIN AGAR & MODIFIED THAYER AGAR and TRYPTIC SOY AGAR W/5% SHEEP BLOOD.

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

Information

FDA registration
United States(from the FDA device records)