FDA applicant

Briox Technologies, Inc.

Mchenry, IL6 decisions1979–19820 recalls

FDA records 6 decisions for Briox Technologies, Inc. (Mchenry, IL) from 1979 to 1982: 6 510(k) clearances. Most are in product codes JCX (Apparatus, Suction, Ward Use, Portable…) and BZQ (Monitor, Breathing Frequency). 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, general and plastic surgery panel, where it files most

How often FDA has decided Briox Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Briox Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Briox Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?