510(k) Report

FDA applicant

Chicago X-Ray Systems, Inc.

Wheeling, IL4 decisions1994–19970 recalls

FDA records 4 decisions for Chicago X-Ray Systems, Inc. (Wheeling, IL) from 1994 to 1997: 4 510(k) clearances. Most are in product codes EAP (Unit, X-Ray, Intraoral) and EHD (Unit, X-Ray, Extraoral With Timer). 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, dental panel, where it files most

How often FDA has decided Chicago X-Ray Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chicago X-Ray Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Chicago X-Ray Systems, Inc.’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 “Chicago”

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