FDA applicant

Medsonics

Mchenry, IL4 decisions1976–19770 recalls

FDA records 4 decisions for Medsonics (Mchenry, IL) from 1976 to 1977: 4 510(k) clearances. Most are in product codes KNG (Monitor, Ultrasonic, Fetal) and JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Medsonics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medsonics

Which product codes does it file in?

What has FDA decided for it lately?