FDA applicant

In-X Corp.

Denver, CO3 decisions2000–20050 recalls

FDA records 3 decisions for In-X Corp. (Denver, CO) from 2000 to 2005: 3 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and DQA (Oximeter). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “In-X Corporation”.

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 In-X Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for In-X Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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In-X 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?