FDA applicant

Marcon Group, Inc.

Washington, DC1 decision1996–19960 recalls

FDA records 1 decision for Marcon Group, Inc. (Washington, DC) in 1996: 1 510(k) clearance. All are in product code FNM (Mattress, Air Flotation, Alternating Pressure). 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 Marcon Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marcon Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Marcon”

FDA records each applicant name separately; these may or may not be the same firm.

Marcon Hearing Instruments, Inc. 10 Marcon Rubber Industry Sdn. Bhd. 1

Marcon Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Marcon”