FDA applicant
Oxoid, Ltd.
FDA records 36 decisions for Oxoid, Ltd. (Basingstoke, GB) from 1997 to 2007: 36 510(k) clearances. Most are in product codes JTN (Susceptibility Test Discs, Antimicrobial) and JWX (Kit, Screening, Staphylococcus Aureus). 6 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Oxoid, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2007
2026 so far, outlined.
Recalls per year
1in 2024
Class I Class II/III not classified
Planning a device like Oxoid, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Oxoid”
FDA records each applicant name separately; these may or may not be the same firm.