510(k) Report

FDA applicant

Narishige Co., Ltd.

Setagaya-Ku, Tokyo, JP20 decisions2000–20120 recalls

FDA records 20 decisions for Narishige Co., Ltd. (Setagaya-Ku, Tokyo, JP) from 2000 to 2012: 20 510(k) clearances. All are in product code MQJ (Micromanipulators And Microinjectors, Assisted…). Its devices cite 3 predicates, 3 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 Narishige Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2012: 2
2007high 2 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Narishige Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Narishige Co., Ltd.’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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