FDA applicant

Advance Tech Intl.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Advance Tech Intl. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code DRX (Electrode, Electrocardiograph). 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 Advance Tech Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advance Tech Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Advance”

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

Advance Medical Designs, Inc. 32 Advance Suture, Inc. 5 Advance Medical Device, Inc. 5 Advance Rubber, Inc. 3 Advance Sentry Corporation 1 Advance Corp. 1

Advance Tech Intl.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Advance”