FDA applicant

Nicolet Biomedical Instruments

Mchenry, IL26 decisions1977–19880 recalls

FDA records 26 decisions for Nicolet Biomedical Instruments (Mchenry, IL) from 1977 to 1988: 26 510(k) clearances. Most are in product codes IKN (Electromyograph, Diagnostic) and GWK (Conditioner, Signal, Physiological). 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, neurology panel, where it files most

How often FDA has decided Nicolet Biomedical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nicolet Biomedical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Nicolet”

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

Nicolet Biomedical, Inc. 18 Nicolet Instrument Corp. 13

Nicolet Biomedical Instruments

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Nicolet”