FDA applicant

Kingston Technologies, Inc.

Dayton, NJ6 decisions1988–19940 recalls

FDA records 6 decisions for Kingston Technologies, Inc. (Dayton, NJ) from 1988 to 1994: 6 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and MGP (Dressing, Wound And Burn, Occlusive). 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 Kingston Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kingston Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kingston Technologies, Inc.

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?