510(k) Report

FDA applicant

Fsusen Technology Co., Ltd.

Shenzhen, CN1 decision2019–20190 recalls

FDA records 1 decision for Fsusen Technology Co., Ltd. (Shenzhen, CN) in 2019: 1 510(k) clearance. All are in product code MUH (System, X-Ray, Extraoral Source, Digital). 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, dental panel, where it files most

How often FDA has decided Fsusen Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019: 1
2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Fsusen Technology Co., Ltd. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MUHSystem, X-Ray, Extraoral Source, Digital1decision

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.

  • K192766Digital Intraoral Imaging Plate SystemFsusen Technology Co., Ltd. · 20191cites it

What has FDA decided for it lately?

  • K192766Digital Intraoral Imaging Plate SystemFsusen Technology Co., Ltd. · 2019

The one decision as Fsusen Technology Co., Ltd. →