R. Kent Richards, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 12
What R. Kent Richards, Inc. makes
R. Kent Richards, Inc. manufactures microbiological culture media and transport media for clinical and diagnostic testing, including selective and differential agars such as Tryptic Soy Blood Agar, Columbia 5% Blood Agar, and Mannitol Salt Agar. Their portfolio also includes specialized media like Thayer-Martin Medium (Modified) for sexually transmitted pathogen isolation and Chlamydia & Viral Transport Medium for specimen preservation. Additional products include diagnostic media for anaerobic bacteria, Campylobacter, and enteric pathogens, such as CDC Anaerobe Blood Agar and Hektoen Enteric Agar.
The company’s products are regulated under FDA’s Class I and Class II device classifications, with many cleared via the 510(k) pathway. These media are listed in the FDA’s 510(k) database, reflecting their authorization for clinical use in the United States. The manufacturer operates from the US.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does R. Kent Richards, Inc. have in the registry?
The registry currently lists 12 devices for R. Kent Richards, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list R. Kent Richards, Inc.'s devices?
Among its 12 most recently registered devices, R. Kent Richards, Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do R. Kent Richards, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for R. Kent Richards, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from R. Kent Richards, Inc. in the registry?
The most recently registered devices listed for R. Kent Richards, Inc. include COLUMBIA CNA AGAR W/5% SHEEP BLOOD, TRYPTIC SOY BLOOD AGAR, CHLAMYDIA & VIRAL TRANSPORT MEDIUM and CDC ANAEROBE BLOOD AGAR.