510(k) Report

FDA applicant

Rowan Products, Inc.

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Rowan Products, Inc. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code GXB (Esthesiometer). 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 Rowan Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rowan Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Rowan Products, 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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