FDA applicant

Menicon U.S.A., Inc.

Washington, DC3 decisions1997–20000 recalls

FDA records 3 decisions for Menicon U.S.A., Inc. (Washington, DC) from 1997 to 2000: 3 510(k) clearances. Most are in product codes HQD (Lens, Contact (Other Material) - Daily) and LPL (Lenses, Soft Contact, Daily Wear). 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 Menicon U.S.A., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Menicon U.S.A., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Menicon U.S.A., 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 “Menicon”

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

Menicon Co, Ltd. 21 Menicon Co., Ltd. New Business Division 1

Menicon U.S.A., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Menicon”