510(k) Report

FDA applicant

Rosch AG Medizintechnic

Berlin, DE1 decision2002–20020 recalls

FDA records 1 decision for Rosch AG Medizintechnic (Berlin, DE) in 2002: 1 510(k) clearance. All are in product code KZE (Injector, Fluid, Non-Electrically Powered). Its devices cite 4 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Rosch AG Medizintechnic since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rosch AG Medizintechnic 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?

  • KZEInjector, Fluid, Non-Electrically Powered1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K020786Injex Needle-Free Injection System; Rojex Needle-Free Injection SystemRosch AG Medizintechnic · 2002

The one decision as Rosch AG Medizintechnic →