FDA device listing
Scenium,Scenium VE30,syngo.MI Cardiology,syngo.MI Neurology,syngo.MI Reading,syngo.MM Oncology,syngo.NM Reading,syngo…
FDA device listing 1072889996 · SIEMENS MEDICAL SOLUTIONS USA, INC.
Key facts
| Proprietary names | Scenium,Scenium VE30,syngo.MI Cardiology,syngo.MI Neurology,syngo.MI Reading,syngo.MM Oncology,syngo.NM Reading,syngo PET&CT Oncology,syngo.PET & CT Oncology,syngo.SPECT Processing,syngo.SPECT Reading,syngo.via MI Workflows,syngo.via MI Workflows VB40A |
|---|---|
| Owner/operator | SIEMENS MEDICAL SOLUTIONS USA, INC. |
| Owner/operator number | 9002915 |
| Premarket submissions | K191309 |
| Product codes | LLZ |
| Device names | LLZ - System, Image Processing, Radiological |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.2050 |
| Review panels | Radiology |
| Registered establishments | SIEMENS MEDICAL SOLUTIONS USA, INC. |
| Establishment registrations | 1423253 |
| FEI numbers | 1000514697 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database