510(k) Report

FDA applicant

Inventive Medical Technology

Trappe, MD1 decision1997–19970 recalls

FDA records 1 decision for Inventive Medical Technology (Trappe, MD) in 1997: 1 510(k) clearance. All are in product code HEX (Colposcope (And Colpomicroscope)). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Inventive Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HEXColposcope (And Colpomicroscope)1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K963593Imt Loupe-ColposcopeInventive Medical Technology · 19971cites it

What has FDA decided for it lately?

  • K963593Imt Loupe-ColposcopeInventive Medical Technology · 1997

The one decision as Inventive Medical Technology →

Other applicant names beginning “Inventive”

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

Inventive Products, Inc. 3Inventive Resources, Inc. 1Inventive Technology Int'L., Inc. 1