FDA applicant

Midwest Marketing Service

Klemme, IA1 decision1986–19860 recalls

FDA records 1 decision for Midwest Marketing Service (Klemme, IA) in 1986: 1 510(k) clearance. All are in product code FTC (Light, Ultraviolet, Dermatological). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Midwest Marketing Service since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Midwest Marketing Service 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 Marketing Service

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”