FDA applicant

Mennen Greatbatch Electonics

Mchenry, IL6 decisions1977–19770 recalls

FDA records 6 decisions for Mennen Greatbatch Electonics (Mchenry, IL) in 1977: 6 510(k) clearances. Most are in product codes DXJ (Display, Cathode-Ray Tube, Medical) and GWQ (Full-Montage Standard Electroencephalograph). 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, cardiovascular panel, where it files most

How often FDA has decided Mennen Greatbatch Electonics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mennen Greatbatch Electonics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mennen”

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

Mennen Medical, Inc. 55

Mennen Greatbatch Electonics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mennen”