FDA applicant

Ethox International

Buffalo, NY1 decision2006–20060 recalls

FDA records 1 decision for Ethox International (Buffalo, NY) in 2006: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). 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, cardiovascular panel, where it files most

How often FDA has decided Ethox International’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ethox International since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ethox”

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

Ethox Corp. 19

Ethox International

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Ethox”