510(k) Report

FDA applicant

Nurion Industries

Paoli, PA3 decisions1990–19910 recalls

FDA records 3 decisions for Nurion Industries (Paoli, PA) from 1990 to 1991: 3 510(k) clearances. All are in product code HPG (Aid, Vision, Electronic, Battery-Powered). 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 Nurion Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nurion Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HPGAid, Vision, Electronic, Battery-Powered3decisions

What has FDA decided for it lately?

  • K910601PathfinderNurion Industries · 1991
  • K903558Laser CaneNurion Industries · 1990
  • K902187PolaronNurion Industries · 1990

All 3 as Nurion Industries →