Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Ventrex with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2006: FEATHERLITE AQUA TOCODYNAMOMETER.
| Jul 12, 2006 | FEATHERLITE AQUA TOCODYNAMOMETERK061044 · HFM | 510(k) clearances |
| Jan 17, 2002 | TOCO LITE, MODEL TD-01K013477 · HFM | 510(k) clearances |
| Jul 16, 1997 | COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67K964821 · DQA | 510(k) clearances |
| Nov 25, 1996 | VENTREX OXYGEN SENSORK963415 · CCL | 510(k) clearances |
| May 14, 1993 | VENTREX ALLERGEN DISCK925044 · DHB | 510(k) clearances |
| Nov 30, 1992 | VENTREX ALLERGEN DISCK924119 · DHB | 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
