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 13, 2026, FDA's public records list Innotron Diagnostics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 12, 1985: INNOFLUOR THEOPHYLLINE.
| Date | Record | Source |
|---|---|---|
| Mar 12, 1985 | INNOFLUOR THEOPHYLLINEK850629 · LGS | 510(k) clearances |
| Jan 8, 1985 | INNOFLUOR PRIMIDONEK844721 · LKT | 510(k) clearances |
| May 31, 1984 | INNOFLOUR TOBRAMYCINK841866 · LFW | 510(k) clearances |
| May 31, 1984 | INNOFLOUR GENTAMICINK841865 · LCQ | 510(k) clearances |
| May 23, 1984 | INNOFLUOR PHENOBARBITALK841707 · LGQ | 510(k) clearances |
| May 22, 1984 | INNOFLUOR PHENYTOINK841706 · LGR | 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
