MeVis Medical Solutions AG
FDA Regulatory Profile
MeVis Medical Solutions AG appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 30, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K260576 | MeVis AVM Contour | June 30, 2026 |
| K232045 | MeVis Liver Suite | October 27, 2023 |
| K201501 | Veolity | February 23, 2021 |
| K120207 | VISIA | April 23, 2012 |
| K120484 | VISIA ONCOLOGY | March 27, 2012 |
| K113701 | VISIA NEURO | February 16, 2012 |
| K113337 | VISIA DYNAMIC REVIEW | December 30, 2011 |