FDA applicant

Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg

Charleston, SC2 decisions2006–20108 recalls

FDA records 2 decisions for Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg (Charleston, SC) from 2006 to 2010: 2 510(k) clearances. All are in product code FSY (Light, Surgical, Ceiling Mounted). Its devices cite 3 predicates, 1 of them its own earlier devices. 8 recalls are 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 Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

5in 2015

2007high 5 (2015) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Trumpf Kreuzer Medizin Systeme 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 “Trumpf”

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

Trumpf Medical Systems, Inc. 1 Trumpf Medizin Systeme GmbH + Co. KG 1

Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg

Which product codes does it file in?

Whose devices does it build on?

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Which of its devices are cited most?

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Other applicant names beginning “Trumpf”