FirmLabelled 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 LonzaLabelled by claude-sonnet-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 15, 2026, FDA's public records list M.A. Bioproducts with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 26, 1983: HERPELISA KIT.
| Jul 26, 1983 | HERPELISA KITK822883 · LGC | 510(k) clearances |
| May 25, 1983 | MYCOPLASMELISA TEST KITK823804 · LJZ | 510(k) clearances |
| May 13, 1983 | MUMPSELISA TEST KITK830045 · LJY | 510(k) clearances |
| May 9, 1983 | CYTOMEGELISA STATK830615 · LFZ | 510(k) clearances |
| May 5, 1983 | VARICELISA TEST KITK823805 · LFY | 510(k) clearances |
| Aug 3, 1982 | CHLAMYDELISA TEST KITK821967 · LJC | 510(k) clearances |
| Jul 30, 1982 | MEASELISA TEST KITK821762 · LJB | 510(k) clearances |
| Jan 26, 1982 | TOXOELISA TEST KITK813221 · LGD | 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
