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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Ventrex Laboratories with 82 510(k) clearances. The most recent is a 510(k) clearance dated Mar 13, 1992: SPECIFIC IGE EIA-TURBO ASSAY.
| Date | Record | Source |
|---|---|---|
| Mar 13, 1992 | SPECIFIC IGE EIA-TURBO ASSAYK914554 · DHB | 510(k) clearances |
| Feb 21, 1992 | VENTREX ALLERGEN DISCK913833 · DHB | 510(k) clearances |
| Oct 25, 1991 | VENTREX COATED TUBE INTACT PTHK913434 · CEW | 510(k) clearances |
| Feb 21, 1991 | VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905612 · DGC | 510(k) clearances |
| Feb 7, 1991 | VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905636 · DHB | 510(k) clearances |
| Jan 17, 1991 | SHBG IRMA KITK905247 · CDZ | 510(k) clearances |
| Dec 7, 1990 | TURBO-RAST SPECIFIC IGE ASSAYK904330 · DHB | 510(k) clearances |
| Jul 31, 1990 | TURBO-RAST SPECIFIC IGE ASSAYK903000 · JHR | 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
