510(k) Report

FDA applicant

Materials Conversion Corp.

Wheeling, IL1 decision1995–19950 recalls

FDA records 1 decision for Materials Conversion Corp. (Wheeling, IL) in 1995: 1 510(k) clearance. All are in product code HET (Laparoscope, Gynecologic (And Accessories)). 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 Materials Conversion Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Materials Conversion Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Materials Conversion Corp. 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?

  • HETLaparoscope, Gynecologic (And Accessories)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K952889Insul-Coat/2 Ceramic Coated Endo Medical InstrumentsMaterials Conversion Corp. · 19952cite it

What has FDA decided for it lately?

  • K952889Insul-Coat/2 Ceramic Coated Endo Medical InstrumentsMaterials Conversion Corp. · 1995

The one decision as Materials Conversion Corp. →