FDA applicant

Midwest Dental Products Corp.

Des Plaines, IL5 decisions1996–19983 recalls

FDA records 5 decisions for Midwest Dental Products Corp. (Des Plaines, IL) from 1996 to 1998: 5 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and KOJ (Airbrush). 3 recalls are 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 Midwest Dental Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest Dental Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Midwest Dental Products 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 “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 Reprocessing Center, LLC 4 Midwest Metabolic Support Group 4 Midwest X-Ray Equipment Co. 3 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 Dental Products Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Midwest”