510(k) Report

FDA applicant

Alain Machtelinckx

West Linn, OR1 decision1994–19940 recalls

FDA records 1 decision for Alain Machtelinckx (West Linn, OR) in 1994: 1 510(k) clearance. All are in product code LYG (Massager, Therapeutic, Manual). 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 Alain Machtelinckx’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alain Machtelinckx since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alain Machtelinckx 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?

  • LYGMassager, Therapeutic, Manual1decision

What has FDA decided for it lately?

  • K930613Hooking SystemAlain Machtelinckx · 1994

The one decision as Alain Machtelinckx →