FDA applicant

Reimers and Janssen GmbH

Waldkirch, Baden Wurthemberg, DE2 decisions2009–20140 recalls

FDA records 2 decisions for Reimers and Janssen GmbH (Waldkirch, Baden Wurthemberg, DE) from 2009 to 2014: 2 510(k) clearances. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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 Reimers and Janssen GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Reimers and Janssen GmbH by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Reimers”

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

Reimers Systems, Inc. 5 Reimers Engineering, Inc. 1

Reimers and Janssen GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reimers”