510(k) Report

FDA applicant

Pin Dot Products, Inc.

Niles, IL14 decisions1991–19930 recalls

FDA records 14 decisions for Pin Dot Products, Inc. (Niles, IL) from 1991 to 1993: 14 510(k) clearances. Most are in product codes KNN (Components, Wheelchair) and JFC (System, Pressure Measurement, Intermittent). 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, physical medicine panel, where it files most

How often FDA has decided Pin Dot Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pin Dot Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pin Dot 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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