510(k) Report

FDA applicant

Levo USA

Dottikon, CH4 decisions1996–19970 recalls

FDA records 4 decisions for Levo USA (Dottikon, CH) from 1996 to 1997: 4 510(k) clearances. All are in product code IPL (Wheelchair, Standup). 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 Levo USA’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Levo USA since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Levo USA by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IPLWheelchair, Standup4decisions

Who builds on its devices?

Later devices cite its devices 6 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K963817Levo Mobil LCMLevo USA · 19975cite it
  • K971873Levo Active-Easy LaeLevo USA · 19971cites it

What has FDA decided for it lately?

  • K973951Levo Compact-Easy LceLevo USA · 1997
  • K963817Levo Mobil LCMLevo USA · 1997
  • K971873Levo Active-Easy LaeLevo USA · 1997
  • K963816Levo Compact LCLevo USA · 1996

All 4 as Levo USA →

Other applicant names beginning “Levo”

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

Levo AG 4Levo Medical Corporation 1