FDA applicant

Greene & Kellogg, Inc.

Mchenry, IL4 decisions1980–19830 recalls

FDA records 4 decisions for Greene & Kellogg, Inc. (Mchenry, IL) from 1980 to 1983: 4 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and BTI (Compressor, Air, Portable). 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 Greene & Kellogg, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Greene & Kellogg, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Greene & Kellogg, 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 “Greene”

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

Greene International Corp. 8

Greene & Kellogg, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Greene”