FDA applicant

Intec.

Blue Springs, MO3 decisions1981–19820 recalls

FDA records 3 decisions for Intec. (Blue Springs, MO) from 1981 to 1982: 3 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) 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 Intec.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intec. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Intec.”

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

Intec Medical, Inc. 17 Intec Industries, Inc. 2

Intec.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intec.”