FDA applicant

Midwest Development

Egale, WI1 decision2005–20050 recalls

FDA records 1 decision for Midwest Development (Egale, WI) in 2005: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, Powered). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, physical medicine panel, where it files most

How often FDA has decided Midwest Development’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest Development since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Midwest Development 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 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 Development

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”