FDA applicant

Marcon Hearing Instruments, Inc.

Mchenry, IL10 decisions1979–19820 recalls

FDA records 10 decisions for Marcon Hearing Instruments, Inc. (Mchenry, IL) from 1979 to 1982: 10 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

How often FDA has decided Marcon Hearing Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marcon Hearing Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Marcon Hearing Instruments, 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 Rubber Industry Sdn. Bhd. 1 Marcon Group, Inc. 1

Marcon Hearing Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Marcon”