FDA applicant

Midwest Reprocessing Center, LLC

Birmingham, AL4 decisions2010–20110 recalls

FDA records 4 decisions for Midwest Reprocessing Center, LLC (Birmingham, AL) from 2010 to 2011: 4 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and NMD (Oximeter, Tissue Saturation, Reprocessed). Its devices cite 46 predicates, 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2011

2010high 3 (2010) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Midwest Reprocessing Center, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Midwest Reprocessing Center, LLC’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 13 Midwest City Hearing Aid Center 12 Midwest Rf, LLC 9 Midwest Orthodontic Mfg. 7 Midwest Dental Products Corp. 5 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 Reprocessing Center, LLC

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”