Medical device makerLabelled 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 13, 2026, FDA's public records list Granbio, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 15, 1996: EBNA ENZYME IMMUNOASSAY KIT.
| Date | Record | Source |
|---|---|---|
| Feb 15, 1996 | EBNA ENZYME IMMUNOASSAY KITK951822 · LLM | 510(k) clearances |
| Apr 20, 1994 | UNKNOWNK934774 · LSE | 510(k) clearances |
| Sep 12, 1990 | EIA FOR IGG ANTIBODY TO EBV VCA IN HUMAN SERUMK901156 · GNP | 510(k) clearances |
| Sep 12, 1990 | (EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUMK901840 · LJN | 510(k) clearances |
| Jun 7, 1988 | INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAYK881617 · LSE | 510(k) clearances |
| Jun 25, 1987 | EBNA ACIF ASSAY KITK871298 · LLM | 510(k) clearances |
| Feb 2, 1987 | INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCAK864347 · GNP | 510(k) clearances |
| Feb 2, 1987 | EBV VCA IGM ANTIBODY ASSAY KITK864604 · LJN | 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
