510(k) Report

FDA applicant

Bel-Art Products

Mchenry, IL3 decisions1977–19810 recalls

FDA records 3 decisions for Bel-Art Products (Mchenry, IL) from 1977 to 1981: 3 510(k) clearances. Most are in product codes IQI (Orthosis, Limb Brace) and ISD (Exerciser, Measuring). 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 Bel-Art Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bel-Art Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bel-Art Products 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?

  • IQIOrthosis, Limb Brace1decision
  • ISDExerciser, Measuring1decision
  • JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use1decision

What has FDA decided for it lately?

  • K813524CentidiscBel-Art Products · 1981
  • K770167Knee SeparatorBel-Art Products · 1977
  • K770164Finger Muscle TesterBel-Art Products · 1977

All 3 as Bel-Art Products →