510(k) Report

FDA applicant

D-View Display Technology Co., Ltd.

Bei Jing, CN1 decision2015–20150 recalls

FDA records 1 decision for D-View Display Technology Co., Ltd. (Bei Jing, CN) in 2015: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

How often FDA has decided D-View Display Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — D-View Display Technology Co., Ltd. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like D-View Display Technology 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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Which product codes does it file in?

  • LLZSystem, Image Processing, Radiological1decision

Whose devices does it build on?

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

What has FDA decided for it lately?

  • K1518543MP (X213C3P0E, X213G3P0E) and 2MP (X213C2P0E, X213G2P0E) LCD DisplayD-View Display Technology Co., Ltd. · 2015

The one decision as D-View Display Technology Co., Ltd. →