FDA applicant

Midwest Eye Laboratories, Inc.

Minneapolis, MN2 decisions1991–19910 recalls

FDA records 2 decisions for Midwest Eye Laboratories, Inc. (Minneapolis, MN) in 1991: 2 510(k) clearances. Most are in product codes HQH (Eye, Artificial, Non-Custom) and HQT (Shell, Scleral). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Midwest Eye Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Midwest Eye Laboratories, Inc. 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 Ophthalmic Instruments, Inc. 1 Midwest Marketing Service 1

Midwest Eye Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Midwest”