Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Thermo Fisher ScientificLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Oxoid USA with 93 510(k) clearances. The most recent is a 510(k) clearance dated Jun 9, 1989: LISTERIA SELECTIVE ENRICHMENT MEDIUM.
| Jun 9, 1989 | LISTERIA SELECTIVE ENRICHMENT MEDIUMK891593 · JSI | 510(k) clearances |
| Feb 3, 1989 | ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KITK884026 · GNA | 510(k) clearances |
| Oct 25, 1988 | LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)K884208 · KZI | 510(k) clearances |
| Nov 6, 1987 | STAPHYLASE TESTK874303 · LHT | 510(k) clearances |
| Aug 10, 1987 | SORBITOL MACCONKEY AGAR NO. 3 CM 813K872956 · JSI | 510(k) clearances |
| Jun 15, 1987 | MCBRIDE MEDIUM CM 819K872135 · JSJ | 510(k) clearances |
| Jun 10, 1987 | RABBIT PLASMA FIBRINOGEN SUPPLEMENT SR 122K870945 · JTL | 510(k) clearances |
| Nov 5, 1986 | OXOID SIGNAL BLOOD CULTURE SYSTEMK862946 · JSG | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
