FDA applicant

Zimmer Medizinsystems GmbH

Neu-Elm, DE2 decisions2012–20140 recalls

FDA records 2 decisions for Zimmer Medizinsystems GmbH (Neu-Elm, DE) from 2012 to 2014: 2 510(k) clearances. Most are in product codes ILY (Lamp, Infrared, Therapeutic Heating) and IMG (Stimulator, Ultrasound And Muscle, For Use In…). Its devices cite 5 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, physical medicine panel, where it files most

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

FDA decisions per year

1in 2014

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Zimmer Medizinsystems GmbH by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Zimmer Medizinsystems GmbH’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 “Zimmer”

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

Zimmer, Inc. 426 Zimmer Spine, Inc. 44 Zimmer Dental, Inc. 40 Zimmer Biomet Spine, Inc. 15 Zimmer Medizinsysteme GmbH 13 Zimmer Trabecular Metal Technology 13 Zimmer Elektromedizin GmbH 12 Zimmer Trabecular 10 Zimmer Biomet 6 Zimmer Switzerland Manufacturing GmbH 4 Zimmer Patient Care Division 3 Zimmer Cas 3

Zimmer Medizinsystems GmbH

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 “Zimmer”