Oxoid U.S.A., Inc.
Country not established
- Devices
- 93
What Oxoid U.S.A., Inc. makes
Oxoid U.S.A., Inc. manufactures diagnostic reagents and culture media for microbiological testing, including selective agar bases, broth bases, supplement discs, and test kits for pathogens such as Campylobacter, Listeria, and Staphylococcus. Specific products include Campylobacter blood-free selective agar base, Selenite cystine broth base, Staphylase test, X-factor discs, rabbit plasma fibrinogen supplement, and various diagnostic discs and reagent sets for agglutination and identification purposes.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's 510(k) registry. Oxoid U.S.A., Inc. is based in the United States.
Catalogue
Search and filter all 93 devicesShowing 1-50 of 93
Frequently asked questions
How many devices does Oxoid U.S.A., Inc. have in the registry?
The registry currently lists 93 devices for Oxoid U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxoid U.S.A., Inc.'s devices?
Among its 50 most recently registered devices, Oxoid U.S.A., Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Oxoid U.S.A., Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Oxoid U.S.A., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxoid U.S.A., Inc. in the registry?
The most recently registered devices listed for Oxoid U.S.A., Inc. include CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASE, CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ, SELENITE CYSTINE BROTH BASE and DIAGNOSTIC REAGENT SET-RPLA.