FDA applicant

Interventional Innovations Corp.

St. Paul, MN2 decisions1996–19970 recalls

FDA records 2 decisions for Interventional Innovations Corp. (St. Paul, MN) from 1996 to 1997: 2 510(k) clearances. All are in product code KRA (Catheter, Continuous Flush). 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 Interventional Innovations Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interventional Innovations Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Interventional”

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

Interventional Therapeutics Corp. 28 Interventional Spine, Inc. 8 Interventional Medical, Inc. 4 Interventional Concepts, Inc. 1 Interventional Research Technologies 1 Interventional Thermodynamics, Inc. 1

Interventional Innovations Corp.

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 “Interventional”