FDA applicant

Midwest

Mchenry, IL13 decisions1976–19860 recalls

FDA records 13 decisions for Midwest (Mchenry, IL) from 1976 to 1986: 13 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EAY (Light, Fiber Optic, Dental). 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 Midwest’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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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 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 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

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?

Other applicant names beginning “Midwest”