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 Immuno-Products Industries with 12 510(k) clearances. The most recent is a 510(k) clearance dated Sep 19, 1985: IMMUNO-PROD IND FLUORE TREPONE ANTIBODY ABSORPED.
| Sep 19, 1985 | IMMUNO-PROD IND FLUORE TREPONE ANTIBODY ABSORPEDK853122 · GMS | 510(k) clearances |
| Jul 10, 1985 | ANA/LITE-HEP-2 TEST SYSTEMK852231 · LJM | 510(k) clearances |
| Jul 10, 1985 | ANA/LITE-RL TEST SYSTEMK852230 · LJM | 510(k) clearances |
| Oct 31, 1984 | FLUORESCENT TREPONEMEL ANTIBODY-ABSORBK843613 · GMS | 510(k) clearances |
| Apr 27, 1983 | ANTINUCLEAR ANTIBODY TISSUE CULTURE SUBK831054 · DHN | 510(k) clearances |
| Mar 24, 1983 | ANTI N DNA-HCPK830652 · KTL | 510(k) clearances |
| Jun 10, 1982 | ANTINUCLEAR ANTIBODY SCREEN FLOURESCK821576 · DBL | 510(k) clearances |
| May 1, 1981 | ANTITHYROID ANTIBODY IMMUNOFLUORESCENTK810982 · JZO | 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
