510(k) Report

FDA applicant

Futuro Div. Jung Corp.

Mchenry, IL2 decisions1983–19830 recalls

FDA records 2 decisions for Futuro Div. Jung Corp. (Mchenry, IL) in 1983: 2 510(k) clearances. All are in product code DWL (Stocking, Medical Support (To Prevent Pooling…). 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, general hospital panel, where it files most

How often FDA has decided Futuro Div. Jung Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Futuro Div. Jung Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Futuro Div. Jung Corp. 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?

  • DWLStocking, Medical Support (To Prevent Pooling Of Blood In Legs)2decisions

Who builds on its devices?

Later devices cite its devices 2 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.

  • K830696Venes Anti Embolism StockingsFuturo Div. Jung Corp. · 19832cite it

What has FDA decided for it lately?

  • K830697Venes High Compression Medical Stock-Futuro Div. Jung Corp. · 1983
  • K830696Venes Anti Embolism StockingsFuturo Div. Jung Corp. · 1983

All 2 as Futuro Div. Jung Corp. →