FDA applicant

Storz Medical AG

Tagerwilen, CH4 decisions2016–20210 recalls

FDA records 4 decisions for Storz Medical AG (Tagerwilen, CH) from 2016 to 2021: 3 510(k) clearances and 1 original PMA approval. Most are in product codes NBN (Generator, Shock-Wave, For Pain Relief) and IPF (Stimulator, Muscle, Powered). Its devices cite 6 predicates, 0 of them its own earlier 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, general and plastic surgery panel, where it files most

How often FDA has decided Storz Medical AG’s devices, and how often a recall has named them.

FDA decisions per year

2in 2021

2016high 2 (2021) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

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

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

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Other applicant names beginning “Storz”

FDA records each applicant name separately; these may or may not be the same firm.

Storz Instrument Co. 101 Storz 6 Storz Ophthalmics, Inc. 4 Storz AM Mark GmbH 2

Storz Medical AG

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Storz”