FDA applicant

Sonometrics Systems, Inc.

Mchenry, IL4 decisions1978–19820 recalls

FDA records 4 decisions for Sonometrics Systems, Inc. (Mchenry, IL) from 1978 to 1982: 4 510(k) clearances. Most are in product codes HLT (Preamplifier, Ac-Powered, Ophthalmic) and IYO (System, Imaging, Pulsed Echo, Ultrasonic). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Sonometrics Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Sonometrics Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?