FDA applicant

Inventive Products, Inc.

Washington, DC3 decisions1995–19970 recalls

FDA records 3 decisions for Inventive Products, Inc. (Washington, DC) from 1995 to 1997: 3 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and IZH (System, X-Ray, Mammographic). Its devices cite 1 predicate, 1 of them its own earlier devices. 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Inventive Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inventive Products, 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 “Inventive”

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

Inventive Medical Technology 1 Inventive Resources, Inc. 1 Inventive Technology Int'L., Inc. 1

Inventive Products, 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 “Inventive”