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 Biorent Diagnostic with 11 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1983: ALBUMIN REAGENT SET.
| Oct 14, 1983 | ALBUMIN REAGENT SETK832747 · CIX | 510(k) clearances |
| Nov 22, 1982 | CK-UV REAGENTK823211 · JHS | 510(k) clearances |
| Nov 22, 1982 | HEMOGLOBIN REAGENTK823060 · KHG | 510(k) clearances |
| Sep 21, 1982 | OPTIMIZED UV-GPT REAGENT SETK822494 · CKA | 510(k) clearances |
| Sep 21, 1982 | OPTIMIZED UV-GOT REAGENT SETK822493 · CIT | 510(k) clearances |
| Sep 17, 1982 | OPTIMIZED UV-LDH REAGENT SETK822492 · CFJ | 510(k) clearances |
| Apr 14, 1982 | COLORIMETRIC LDH REAGENT SETK820768 · CFH | 510(k) clearances |
| Mar 25, 1982 | COLORIMETRIC URIC ACID REAGENT SETK820632 · KNK | 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
