# Vygon Us, LLC

- Location (FDA's records): Norristown, PA
- FDA decisions: 3 (2004–2006): 3 510(k) clearances
- Product codes: JXG (1), LJS (1), FRG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K052475: Vygon Nutriline and Nutriline Twinflow Catheters (Sep 14, 2006)
- K033704: Modification to Lumbo-Peritoneal Shunts and Lumbar Drainage Catheters (May 27, 2004)
- K040707: Packaging Tray and Components (Apr 16, 2004)

Source page: https://510kreport.com/company/vygon-us