FDA applicant

Aplicare, Inc.

Madison, CT9 decisions1983–19940 recalls

FDA records 9 decisions for Aplicare, Inc. (Madison, CT) from 1983 to 1994: 9 510(k) clearances. Most are in product codes LKB (Pad, Alcohol, Device Disinfectant) and NEC (Bandage, Liquid, Skin Protectant). 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 Aplicare, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aplicare, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aplicare, 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?