FDA applicant

Midwest City Hearing Aid Center

Midwest City, OK12 decisions1995–19970 recalls

FDA records 12 decisions for Midwest City Hearing Aid Center (Midwest City, OK) from 1995 to 1997: 12 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

How often FDA has decided Midwest City Hearing Aid Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest City Hearing Aid Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Midwest”

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

Midwest 13 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 City Hearing Aid Center

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”