FDA applicant

Essex Industries, Inc.

St. Louis, MO4 decisions2010–20170 recalls

FDA records 4 decisions for Essex Industries, Inc. (St. Louis, MO) from 2010 to 2017: 4 510(k) clearances. Most are in product codes BYJ (Unit, Liquid-Oxygen, Portable) and ECX (Cylinder, Compressed Gas, And Valve). Its devices cite 3 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, anesthesiology panel, where it files most

How often FDA has decided Essex Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Essex Industries, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Essex Industries, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Essex”

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

Essex Cryogenics of Missouri, Inc. 5 Essex Industries, Inc. D/B/A Essex Cryogenics of M 1 Essex Medical Systems Plus 1

Essex Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Essex”