FDA applicant

The Devilbiss Co.

Somerset, PA12 decisions1977–19870 recalls

FDA records 12 decisions for The Devilbiss Co. (Somerset, PA) from 1977 to 1987: 12 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and CAF (Nebulizer (Direct Patient Interface)). 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 The Devilbiss Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Devilbiss Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “The”

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

Devilbiss Health Care, Inc. 29 Devilbiss Healthcare, LLC 7

The Devilbiss Co.

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 “The”