FDA applicant

Continental X-Ray Corp.

Broadview, IL27 decisions1988–19970 recalls

FDA records 27 decisions for Continental X-Ray Corp. (Broadview, IL) from 1988 to 1997: 27 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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 Continental X-Ray Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Continental X-Ray Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Continental”

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

Continental Medical Laboratories, Inc. 8 Continental Soft Lens, Inc. 2 Continental Optical Imports 2 Continental Dental Laboratory 1 Continental Dental Ceramics, Inc. (Dba Continental 1 Continental Scale Corp. 1 Continental Dental Ceramics, Inc. 1 Continental Products, Inc. 1

Continental X-Ray Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Continental”