Diagnostics makerLabelled 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 Johnson & JohnsonLabelled 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. See the Johnson & Johnson group view.
As of Nov 13, 2026, FDA's public records list Ortho Diagnostics, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Oct 23, 1980: ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE.
| Date | Record | Source |
|---|---|---|
| Oct 23, 1980 | ORTHO BOVINE ALBUMIN SOLUTION 30% PROTEK802404 · DCF | 510(k) clearances |
| Aug 20, 1980 | ANTIGEN CONTROL CELLSK801507 · GOL | 510(k) clearances |
| Apr 16, 1980 | BI-LEVEL ASSAYED CARD. DRUG CONT., I,IIK800357 · LAS | 510(k) clearances |
| Mar 5, 1980 | ORTHO ANTISERA CONTROLK800310 · KSF | 510(k) clearances |
| Oct 11, 1979 | ORTHO ANTIBODY ENHANCEMENT SOLUTIONK791791 · KSG | 510(k) clearances |
| Sep 24, 1979 | ORTHO TSH RIA KITK791301 · JLW | 510(k) clearances |
| Jun 28, 1979 | MULTECON BLOOD GAS CONTROLK790813 · JJS | 510(k) clearances |
| Apr 4, 1979 | PREGNANCY, SENSIDEX TUBE TESTK782063 · JHJ | 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
