FDA applicant

Midwest X-Ray Equipment Co.

Aurora, IL3 decisions1982–19930 recalls

FDA records 3 decisions for Midwest X-Ray Equipment Co. (Aurora, IL) from 1982 to 1993: 3 510(k) clearances. All are in product code KPX (Changer, Radiographic Film/Cassette). 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 Midwest X-Ray Equipment Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest X-Ray Equipment Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Midwest”

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

Midwest 13 Midwest City Hearing Aid Center 12 Midwest Rf, LLC 9 Midwest Orthodontic Mfg. 7 Midwest Dental Products Corp. 5 Midwest Reprocessing Center, LLC 4 Midwest Metabolic Support Group 4 Midwest Analog & Digital, Inc. 3 Midwest Implant Sales, Inc. 3 Midwest Eye Laboratories, Inc. 2 Midwest Ophthalmic Instruments, Inc. 1 Midwest Marketing Service 1

Midwest X-Ray Equipment Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”