FDA applicant

Endosonics Corp.

Rancho Cordova, CA15 decisions1989–20000 recalls

FDA records 15 decisions for Endosonics Corp. (Rancho Cordova, CA) from 1989 to 2000: 15 510(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 Endosonics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endosonics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Endosonics Corp.

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?