FDA applicant

Thyssenkrupp Ceteco Srl

Pisa, IT2 decisions2009–20100 recalls

FDA records 2 decisions for Thyssenkrupp Ceteco Srl (Pisa, IT) from 2009 to 2010: 2 510(k) clearances. All are in product code ING (Elevator, Wheelchair, Portable). Its devices cite 2 predicates, 1 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 Thyssenkrupp Ceteco Srl’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

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

Planning a device like Thyssenkrupp Ceteco Srl’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 “Thyssenkrupp”

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

Thyssenkrupp Accessibility B.V. 2

Thyssenkrupp Ceteco Srl

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Thyssenkrupp”