510(k) Report

FDA applicant

Menicon Co., Ltd. New Business Division

Minneapolis, MN1 decision2014–20140 recalls

FDA records 1 decision for Menicon Co., Ltd. New Business Division (Minneapolis, MN) in 2014: 1 510(k) clearance. All are in product code MQK (Labware, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Menicon Co., Ltd. New Business Division’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Menicon Co., Ltd. New Business Division by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MQKLabware, Assisted Reproduction1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K133295QualisMenicon Co., Ltd. New Business Division · 20141cites it

What has FDA decided for it lately?

  • K133295QualisMenicon Co., Ltd. New Business Division · 2014

The one decision as Menicon Co., Ltd. New Business Division →

Other applicant names beginning “Menicon”

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

Menicon Co, Ltd. 21Menicon U.S.A., Inc. 3