FDA applicant

Isratech Marketing Corp.

New York, NY2 decisions1987–19890 recalls

FDA records 2 decisions for Isratech Marketing Corp. (New York, NY) from 1987 to 1989: 2 510(k) clearances. Most are in product codes KIZ (Dish, Tissue Culture) and KGO (Surgeon'S Gloves). 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, hematology panel, where it files most

How often FDA has decided Isratech Marketing Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Isratech Marketing Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Isratech Marketing Corp.

Which product codes does it file in?

What has FDA decided for it lately?