510(k) Report

FDA applicant

Multigestion (Deutschland) GmbH

Saint Victor De Gessieu, FR1 decision1995–19950 recalls

FDA records 1 decision for Multigestion (Deutschland) GmbH (Saint Victor De Gessieu, FR) in 1995: 1 510(k) clearance. All are in product code KIC (Cushion, Flotation). 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 Multigestion (Deutschland) GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multigestion (Deutschland) GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Multigestion (Deutschland) GmbH 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?

  • KICCushion, Flotation1decision

What has FDA decided for it lately?

  • K950085Multicure (R) S Gel PadMultigestion (Deutschland) GmbH · 1995

The one decision as Multigestion (Deutschland) GmbH →