FDA applicant

Visidyne Corp.

Mchenry, IL3 decisions1981–19810 recalls

FDA records 3 decisions for Visidyne Corp. (Mchenry, IL) in 1981: 3 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and HIT (Tester, Color Vision). 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 Visidyne Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Visidyne Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Visidyne Corp.

Which product codes does it file in?

What has FDA decided for it lately?