FDA applicant

Sontek Industries, Inc.

Mchenry, IL7 decisions1981–19830 recalls

FDA records 7 decisions for Sontek Industries, Inc. (Mchenry, IL) from 1981 to 1983: 7 510(k) clearances. Most are in product codes JAY (Support, Breathing Tube) and BZA (Connector, Airway (Extension)). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Sontek Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sontek”

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

Sontek Corp. 3

Sontek Industries, Inc.

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 “Sontek”