FDA applicant

Everest Biomedical Instruments Co.

Chesterfield, MO2 decisions2003–20060 recalls

FDA records 2 decisions for Everest Biomedical Instruments Co. (Chesterfield, MO) from 2003 to 2006: 2 510(k) clearances. Most are in product codes OLW (Index-Generating Electroencephalograph Software) and EWO (Audiometer). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Everest Biomedical Instruments Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Everest Biomedical Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Everest”

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

Everest & Jennings, Inc. 30 Everest Medical Corp. 21 Everest Interscience, Inc. 1 Everest Spine, LLC 1

Everest Biomedical Instruments Co.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Everest”