FDA applicant

Metatech Corp.

Wheeling, IL16 decisions1985–20040 recalls

FDA records 16 decisions for Metatech Corp. (Wheeling, IL) from 1985 to 2004: 16 510(k) clearances. Most are in product codes GWM (Device, Monitoring, Intracranial Pressure) and GEX (Powered Laser Surgical Instrument). Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Metatech Co., Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Metatech Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metatech Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Metatech Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?