510(k) Report

FDA applicant

Vanaray Laboratories, Inc.

Mchenry, IL10 decisions1980–19810 recalls

FDA records 10 decisions for Vanaray Laboratories, Inc. (Mchenry, IL) from 1980 to 1981: 10 510(k) clearances. Most are in product codes GYB (Media, Electroconductive) 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Vanaray Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vanaray Laboratories, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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