Diagnostics 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 15, 2026, FDA's public records list International Diagnostic Technology with 29 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 1985: FIAX TOXO-M ANTIBODIES TEST KIT.
| Apr 30, 1985 | FIAX TOXO-M ANTIBODIES TEST KITK850591 · GLZ | 510(k) clearances |
| Oct 5, 1984 | FIAX HAPTOGLOBIN TEST KITK843570 · DAB | 510(k) clearances |
| Sep 28, 1984 | FIAX 420 DILUTORK843621 · JQW | 510(k) clearances |
| Sep 17, 1984 | FIAX 100 FLUOROMETERK843356 · JZT | 510(k) clearances |
| Aug 28, 1984 | FIAX TOTAL IGE TEST KITK842749 · DGP | 510(k) clearances |
| Jul 11, 1984 | FIAX TRANSFERRIN TEST KITK842071 · DDI | 510(k) clearances |
| Jun 7, 1984 | RUBELLA ANTIBODY FLUOROIMMUNOASSAYK841174 · GOL | 510(k) clearances |
| May 11, 1984 | ALPHA-1-ANTITRYPSIN, FITC, ANTIGENK840867 · DEI | 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
