# Siemens Medical Solutions USA, Inc. (contract manufacturer, Hoffman Estates, IL): 5 new FDA device listings, incl. automated radiological image processing software

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Siemens Medical Solutions USA, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Hoffman Estates, IL, US |
| New listings | 5 |
| Devices | Automated Radiological Image Processing Software; System, X-Ray, Tomography, Computed; System, Tomography, Computed, Emission; Full Field Digital, System, X-Ray, Mammographic; Digital Breast Tomosynthesis |
| Product codes | QIH, JAK, KPS, MUE, OTE |
| Device classes | Class II, Class III |
| Medical specialties | Radiology |
| Brand names | MI View&Go VA40; MI View&Go; Symbia Pro.specta VA40 Family; Symbia Pro.specta SPEED; Symbia Pro.specta Q3; Symbia Pro.specta X7; Symbia Pro.specta X3; Symbia Pro.specta SHARP |
| First new listing | 2026-05-26 |
| Latest new listing | 2026-07-07 |
| FDA registration number | 1423253 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.