FDA applicant

Atlantic Products, Inc.

Hicksville, NY1 decision2002–20020 recalls

FDA records 1 decision for Atlantic Products, Inc. (Hicksville, NY) in 2002: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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 Atlantic Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Atlantic Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Atlantic Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?