Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 3 companies' records, each linked to the record.
As of Nov 13, 2026, FDA's public records list thyssenkrupp and its 3 subsidiaries with 4 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Nov 1, 2012: LEVANT, HOMEGLIDE.
| Date | Record | Source |
|---|---|---|
| Nov 1, 2012 | LEVANT, HOMEGLIDEK121560 · ILK | 510(k) clearances |
| Oct 26, 2012 | FLOW2, SWINGK121561 · ILK | 510(k) clearances |
| Aug 6, 2012 | ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and dClass II · The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the | Device recalls |
| Oct 20, 2010 | JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFTK102088 · ING | 510(k) clearances |
| May 27, 2009 | JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)K090856 · ING | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
