# MeVis Medical Solutions AG

- Location (FDA's records): Pewaukee, WI
- FDA decisions: 7 (2011–2026): 7 510(k) clearances
- Product codes: LLZ (4), LNH (1), JAK (1), OEB (1)
- Predicates its devices cite: 11 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vital Images, Inc.: 2 (https://510kreport.com/company/vital-images)
- R2 Technology, Inc.: 2 (https://510kreport.com/company/r2-technology)
- Siemens Corp.: 1 (https://510kreport.com/company/siemens)
- Siemens Medi Cal Solutions, Inc.: 1 (https://510kreport.com/company/siemens-medi-cal-solutions)
- Microsoft Corp.: 1 (https://510kreport.com/company/microsoft)
- Invivo Corporation: 1 (https://510kreport.com/company/invivo)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)

## Firms that cite its devices most
- Edda Technology, Inc.: 1 (https://510kreport.com/company/edda-technology)
- Dexin Medical Imaging Technology Co., Ltd.: 1 (https://510kreport.com/company/dexin-medical-imaging-technology)
- Fujifilm Meidcal Systems U.S.A.,Inc.: 1 (https://510kreport.com/company/fujifilm-meidcal-systems-usa)

## Its most-cited devices
- K120484: Visia Oncology (2012), cited by 2
- K113701: Visia Neuro (2012), cited by 1

## Recent decisions
- K260576: MeVis AVM Contour (Jun 30, 2026)
- K232045: MeVis Liver Suite (Oct 27, 2023)
- K201501: Veolity (Feb 23, 2021)
- K120207: VISIA (Apr 23, 2012)
- K120484: Visia Oncology (Mar 27, 2012)
- K113701: Visia Neuro (Feb 16, 2012)
- K113337: Visia Dynamic Review (Dec 30, 2011)

Source page: https://510kreport.com/company/mevis-medical-solutions