FDA applicant

Vertex Medical Corp.

Mchenry, IL21 decisions1982–19840 recalls

FDA records 21 decisions for Vertex Medical Corp. (Mchenry, IL) from 1982 to 1984: 21 510(k) clearances. Most are in product codes DXT (Injector And Syringe, Angiographic) and DQO (Catheter, Intravascular, Diagnostic). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Vertex Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Vertex”

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

Vertex-Dental B.V. 8 Vertex Technical Group, Inc. 1

Vertex Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vertex”