510(k) Report

FDA applicant

Friendly Sensors AG

Washington, DC1 decision2004–20040 recalls

FDA records 1 decision for Friendly Sensors AG (Washington, DC) in 2004: 1 510(k) clearance. All are in product code NKI (Goniometer With Electrodes). 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 Friendly Sensors AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Friendly Sensors AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Friendly Sensors AG 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?

  • NKIGoniometer With Electrodes1decision

What has FDA decided for it lately?

  • K033193SonosensFriendly Sensors AG · 2004

The one decision as Friendly Sensors AG →