510(k) Report

FDA applicant

Mindmaze SA

Lausanne, CH2 decisions2017–20180 recalls

FDA records 2 decisions for Mindmaze SA (Lausanne, CH) from 2017 to 2018: 2 510(k) clearances. All are in product code LXJ (Interactive Rehabilitation Exercise Devices). 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 Mindmaze SA’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2017: 12018: 1
2017high 1 (2017) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Mindmaze SA by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mindmaze SA’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • LXJInteractive Rehabilitation Exercise Devices2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K162748MindMotionPROMindmaze SA · 20171cites it

What has FDA decided for it lately?

  • K173931MindMotion (TM) GOMindmaze SA · 2018
  • K162748MindMotionPROMindmaze SA · 2017

All 2 as Mindmaze SA →