FDA applicant

Trex Medical Corp.

Copiague, NY6 decisions1998–19990 recalls

FDA records 6 decisions for Trex Medical Corp. (Copiague, NY) from 1998 to 1999: 6 510(k) clearances. Most are in product codes IZH (System, X-Ray, Mammographic) and IZL (System, X-Ray, Mobile). Its devices cite 4 predicates, 0 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 Trex Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trex Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Trex Medical Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Trex”

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

Trex Enterprises Corp. 1

Trex Medical Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Trex”