FDA applicant

Medibond, Ltd.

Efrat, IL1 decision1997–19970 recalls

FDA records 1 decision for Medibond, Ltd. (Efrat, IL) in 1997: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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, neurology panel, where it files most

How often FDA has decided Medibond, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medibond, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medibond, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?