510(k) Report

FDA applicant

Thyssenkrupp Accessibility B.V.

Zuid-Holland, NL2 decisions2012–20121 recall

FDA records 2 decisions for Thyssenkrupp Accessibility B.V. (Zuid-Holland, NL) in 2012: 2 510(k) clearances. All are in product code ILK (Transport, Patient, Powered). Its devices cite 3 predicates, 0 of them its own earlier devices. 1 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 Accessibility B.V.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2012: 2
2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

1in 2012

2012: 1
2012high 1 (2012) · low 0 (2013)2026

Class I Class II/III not classified

FIG. 1 — Thyssenkrupp Accessibility B.V. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • ILKTransport, Patient, Powered2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K121560Levant, HomeglideThyssenkrupp Accessibility B.V. · 20121 recall
  • K121561FLOW2, SwingThyssenkrupp Accessibility B.V. · 2012

All 2 as Thyssenkrupp Accessibility B.V. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K121560ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one…Aug 6, 2012Class II

Other applicant names beginning “Thyssenkrupp”

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

Thyssenkrupp Ceteco Srl 2