FDA applicant

Intertex Medical

Mchenry, IL2 decisions1983–19950 recalls

FDA records 2 decisions for Intertex Medical (Mchenry, IL) from 1983 to 1995: 2 510(k) clearances. Most are in product codes GBZ (Catheter, Cholangiography) and BZA (Connector, Airway (Extension)). No recall is linked to its devices.

FDA’s records also spell it “Intertex Medical, Inc.”.

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 Intertex Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intertex Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Intertex”

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

Intertex Research, Inc. 1

Intertex Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intertex”