FDA applicant

Migada, Ltd.

Israel, IL16 decisions1985–19960 recalls

FDA records 16 decisions for Migada, Ltd. (Israel, IL) from 1985 to 1996: 16 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and LHI (Set, I.V. Fluid Transfer). No recall is linked to its devices.

FDA’s records also spell it “Migada, Inc.”.

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 Migada, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Migada, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Migada”

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

Migada Plant 3

Migada, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Migada”