# Siemens Medical Soultions USA, Inc.

- Location (FDA's records): Hoffman Estates, IL
- FDA decisions: 3 (2019–2023): 3 510(k) clearances
- Product codes: LLZ (2), JAK (1)
- 510(k) review time since 2016: median 65 days, against 112 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Siemens Healthcare GmbH: 1 (https://510kreport.com/company/siemens-healthcare)

## Firms that cite its devices most
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Its most-cited devices
- K191309: syngo.via MI Workflows VB40A, Scenium (2019), cited by 2

## Recent decisions
- K231351: Chondral Quant (Jul 13, 2023)
- K200515: syngo.CT Cardiac Planning (Mar 25, 2020)
- K191309: syngo.via MI Workflows VB40A, Scenium (Jul 19, 2019)

Source page: https://510kreport.com/company/siemens-medical-soultions-usa