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Oxoid Limited

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Part of Oxoid Ltd

Oxoid Limited is a medical device manufacturer, with 92 devices listed in FDA GUDID and EUDAMED (FDA Class I and II) and 1 FDA recall as of 14 Nov 2026.

Devices
92
FDA recalls
11 ongoing

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 92
  • EUDAMED 46

A device listed in two registries counts in both.

Device classes
  • FDA Class I 48
  • FDA Class II 44
FDA recalls
Sites and related companies
Identifiers
  • DUNS 365355452

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Oxoid Limited makes

Oxoid Limited manufactures in vitro diagnostic (IVD) products for microbiological testing, including culture media supplements, antimicrobial susceptibility testing discs, and serological reagents for identifying bacterial species and toxins. Their portfolio also includes fluorescent immunoassay kits for detecting respiratory viruses, such as parainfluenza and influenza, as well as atmospheric generation kits and software tools for automated identification of bacterial isolates.

The company’s devices are classified under FDA’s Class I and Class II regulatory categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Oxoid Limited operates from the United States, adhering to applicable IVD regulations for diagnostic testing products.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue92

Newest first, rows 1-50 of 92

Search and filter all 92 devices
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  • Thermo Scientific Oxoid Gepotidacin Disc (10 ug) GEP10 CT1975B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Microbact Gnb 24E Tray (40 Id's) MB1131A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CT0794B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Microbact Program For Windows MB1244A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • An-Ident DISCSDD6 6X50 Discs DD0006A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • R2456096

    Listed Registry: GUDID Class:II

  • CT0044B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Clostridium Difficile CM0601B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:I

  • Sul Sulphonamide DD0011T

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • Dryspot Pneumo DR0420M

    Active Regimes: CE IVDR Registry: EUDAMEDGUDID Class:I

  • K610611-2

    Listed Registry: GUDID Class:II

  • Arcobacter Broth CM0965B

    Listed Registry: GUDID Class:I

  • R2454096

    Listed Registry: GUDID Class:II

  • IMAGEN Respiratory Syncytial Virus (RSV) K610211-2

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CT0149B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • R2458096

    Listed Registry: GUDID Class:II

  • IMAGEN Respiratory Screen Kit K612011-2

    Active Regimes: 510(k) Registry: GUDID Class:I

  • CT0005B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Anaerobic Catalyst BR0042A

    Listed Registry: GUDID Class:I

  • CT1647B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • CT0038B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • CT0108B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • IMAGEN Influenza Virus A and B K610511-2

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CM0261B

    Listed Registry: GUDID Class:II

  • CT1650B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Orsab Selective Supplement SR0195E

    Listed Registry: GUDID Class:I

  • CT1894B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Microbact Gnb 12A Strip (60 Id's) MB1132A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • H.pylori Selective Supp.(Dent) SR0147E

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CT1661B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • CT0167B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • XLT-4 Selective Supplement SR0237C

    Listed Registry: GUDID Class:I

  • V.C.N.T. Selective Supplement SR0091H

    Active Regimes: CE IVDR 510(k) Registry: EUDAMEDGUDID Class:I

  • CT0010B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • R2458496

    Listed Registry: GUDID Class:II

  • X & V Factor DD0005B

    Active Regimes: CE IVDR 510(k) Registry: EUDAMEDGUDID Class:I

  • CT0017B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Microbact Staph 12S MB1561A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CT1896B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Microbact Listeria 12l (20 Id's) MB1128A

    Active Regimes: CE IVDD Registry: EUDAMEDGUDID Class:I

  • CT0006B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • CM0471T

    Listed Registry: GUDID Class:II

  • CT1964B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • SET-RPLA, Staphylococcal Enterotoxin Kit, 20 tests TD0900A

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Latex Grouping Reagent B DR0587G

    Active Regimes: CE IVDR Registry: EUDAMEDGUDID Class:I

  • CT0059B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • CT1897B

    Active Regimes: CE IVDD 510(k) Registry: EUDAMEDGUDID Class:II

  • Latex Grouping Reagent D DR0589G

    Active Regimes: CE IVDR Registry: EUDAMEDGUDID Class:I

  • CT1895B

    Active Regimes: 510(k) Registry: GUDID Class:II

  • R2458596

    Listed Registry: GUDID Class:II

Rows 1-50 of 92

Showing 1-50 of 92

Company details

DUNS number
365355452
Phone
+441256694238

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by OXOID LIMITED, initiated on 2024-12-23. By recorded status: 1 ongoing. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination and packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 1
  • 2025 0
  • 2026 0

  • 2024

    • 23 Dec 2024 Z-1075-2025 Class II Ongoing Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may contain Norfloxacin Antimicrobial Susceptibility discs. Distribution: US: VA, CA, NE, MA, FL, CA, MA, NH, WA OUS: Austria, Australia, Brazil, Canada, China, Costa Rica, Germany, Spain,…
      Full distribution text US: VA, CA, NE, MA, FL, CA, MA, NH, WA OUS: Austria, Australia, Brazil, Canada, China, Costa Rica, Germany, Spain, France, United Kingdom, Ghana, Hong Kong, South Korea, Netherlands, Peru, Philippines, Poland, Indonesia
      Submission number: K060286

Frequently asked questions

How many devices does OXOID LIMITED have in the registry?

The registry currently lists 92 devices for OXOID LIMITED. Devices recorded under merged duplicate company entries are counted once.

Which registries list OXOID LIMITED's devices?

Among its 50 most recently registered devices, OXOID LIMITED has devices listed in EUDAMED (29 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do OXOID LIMITED's devices fall under?

Among its 50 most recently registered devices, the classes recorded for OXOID LIMITED's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for OXOID LIMITED?

FDA recall records list 1 recall initiated by OXOID LIMITED, the most recent initiated on 23 Dec 2024. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from OXOID LIMITED in the registry?

The most recently registered devices listed for OXOID LIMITED include Thermo Scientific Oxoid Gepotidacin Disc (10 ug) GEP10 CT1975B, MICROBACT GNB 24E TRAY (40 ID'S) MB1131A, CT0794B and MICROBACT PROGRAM FOR WINDOWS MB1244A.

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