Vygon USA
FDA Regulatory Profile
Vygon USA appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 19, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243361 | Nutrifit | December 19, 2024 |
| K212370 | Leaderflex Mini and Leaderflex Nano | August 29, 2022 |
| K181208 | Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter | November 2, 2018 |
| K172899 | Vygon PICCs | February 26, 2018 |