510(k) Report

FDA applicant

Artscan Medical Innovations

Akron, OH1 decision2001–20010 recalls

FDA records 1 decision for Artscan Medical Innovations (Akron, OH) in 2001: 1 510(k) clearance. All are in product code NGR (Tester, Stiffness, Cartilage, Arthroscopic). 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, orthopedic panel, where it files most

How often FDA has decided Artscan Medical Innovations’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Artscan Medical Innovations since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Artscan Medical Innovations 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?

  • NGRTester, Stiffness, Cartilage, Arthroscopic1decision

What has FDA decided for it lately?

  • K010303Artscan Cartilage Stiffness Testing DeviceArtscan Medical Innovations · 2001

The one decision as Artscan Medical Innovations →