510(k) Report

FDA applicant

Jilco Enterprises

Grandview, MO1 decision2000–20000 recalls

FDA records 1 decision for Jilco Enterprises (Grandview, MO) in 2000: 1 510(k) clearance. All are in product code ITH (Equipment, Traction, Powered). 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 Jilco Enterprises’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jilco Enterprises since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jilco Enterprises 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?

  • ITHEquipment, Traction, Powered1decision

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.

  • K001361Jilco Traction-Flexion ChairJilco Enterprises · 20002cite it

What has FDA decided for it lately?

  • K001361Jilco Traction-Flexion ChairJilco Enterprises · 2000

The one decision as Jilco Enterprises →