FDA applicant

Siemens Ultrasound, Inc.

San Ramon, CA8 decisions1989–19910 recalls

FDA records 8 decisions for Siemens Ultrasound, Inc. (San Ramon, CA) from 1989 to 1991: 8 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and ITX (Transducer, Ultrasonic, Diagnostic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Siemens Ultrasound, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Siemens Ultrasound, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Siemens Ultrasound, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Siemens Ultrasound, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?