Siemens Medical Solutions USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Symbia Pro.specta Q3 (11364751), syngo Application Software, ARTIS icono floor
779
Total
779
Cleared
0
Denied
FDA 510(k) Regulatory Record - Siemens Medical Solutions USA, Inc. Radiology ✕
675 devices
Cleared
May 21, 2026
Symbia Pro.specta Q3 (11364751)
Radiology
30d
Cleared
Apr 29, 2026
syngo Application Software
Radiology
127d
Cleared
Apr 24, 2026
ARTIS icono floor
Radiology
122d
Cleared
Apr 23, 2026
ARTIS genio floor
Radiology
149d
Cleared
Mar 20, 2026
SOMATOM X.cite
Radiology
123d
Cleared
Feb 10, 2026
MI View&GO
Radiology
57d
Cleared
Nov 17, 2025
ACUSON Maple Diagnostic Ultrasound System
Radiology
27d
Cleared
Nov 13, 2025
ACUSON Juniper Diagnostic Ultrasound System
Radiology
38d
Cleared
Nov 04, 2025
Cios Select
Radiology
281d
Cleared
Oct 15, 2025
syngo.CT Dual Energy
Radiology
125d
Cleared
Aug 20, 2025
ACUSON Sequoia Diagnostic Ultrasound System
Radiology
99d
Cleared
Jul 31, 2025
Biograph Trinion
Radiology
71d
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