FDA applicant

Applied Medical Devices, Inc.

Mchenry, IL11 decisions1979–19840 recalls

FDA records 11 decisions for Applied Medical Devices, Inc. (Mchenry, IL) from 1979 to 1984: 11 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). 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 Applied Medical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Applied Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Applied Medical Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?