FDA applicant

Sonicaid, Inc.

Mchenry, IL18 decisions1977–19880 recalls

FDA records 18 decisions for Sonicaid, Inc. (Mchenry, IL) from 1977 to 1988: 18 510(k) clearances. Most are in product codes HGM (System, Monitoring, Perinatal) 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 Sonicaid, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sonicaid, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Sonicaid, Inc.

Which product codes does it file in?

What has FDA decided for it lately?