FDA applicant

Ethox Corp.

Buffalo, NY19 decisions1977–20041 recall

FDA records 19 decisions for Ethox Corp. (Buffalo, NY) from 1977 to 2004: 19 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and DXQ (Blood Pressure Cuff). Its devices cite 2 predicates, 1 of them its own earlier devices. 1 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Ethox Corp. since 2007.

Recalls per year

1in 2011

2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Ethox Corp.’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 “Ethox”

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

Ethox International 1

Ethox Corp.

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?

What has been recalled?

Other applicant names beginning “Ethox”