Medical device 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 VygonLabelled 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 Vygon US with 3 510(k) clearances. The most recent is a 510(k) clearance dated Sep 14, 2006: VYGON NUTRILINE AND NUTRILINE TWINFLOW CATHETERS.
| Date | Record | Source |
|---|---|---|
| Sep 14, 2006 | VYGON NUTRILINE AND NUTRILINE TWINFLOW CATHETERSK052475 · LJS | 510(k) clearances |
| May 27, 2004 | MODIFICATION TO LUMBO-PERITONEAL SHUNTS AND LUMBAR DRAINAGE CATHETERSK033704 · JXG | 510(k) clearances |
| Apr 16, 2004 | PACKAGING TRAY AND COMPONENTSK040707 · FRG | 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
