FDA applicant

Neurotherapies Reset GmbH

Juelich, DE1 decision2016–20160 recalls

FDA records 1 decision for Neurotherapies Reset GmbH (Juelich, DE) in 2016: 1 510(k) clearance. All are in product code KLW (Masker, Tinnitus). 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, ear, nose and throat panel, where it files most

How often FDA has decided Neurotherapies Reset GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Neurotherapies Reset GmbH by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Neurotherapies Reset GmbH

Which product codes does it file in?

What has FDA decided for it lately?