FDA applicant

Citizen Systems Japan Co., Ltd.

Washington, DC4 decisions2010–20100 recalls

FDA records 4 decisions for Citizen Systems Japan Co., Ltd. (Washington, DC) in 2010: 4 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). 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 Citizen Systems Japan Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

4in 2010

2010high 4 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Citizen Systems Japan Co., Ltd. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Citizen Systems Japan Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Citizen”

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

Citizen Watch Co., Ltd. 8

Citizen Systems Japan Co., Ltd.

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 “Citizen”