FDA applicant

Direct Digital Imaging Technology (Beijing), Inc.

Beijing, CN2 decisions2009–20110 recalls

FDA records 2 decisions for Direct Digital Imaging Technology (Beijing), Inc. (Beijing, CN) from 2009 to 2011: 2 510(k) clearances. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/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, radiology panel, where it files most

How often FDA has decided Direct Digital Imaging Technology (Beijing), Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Direct Digital Imaging Technology (Beijing), Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Direct Digital Imaging Technology…’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 “Direct”

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

Direct Solutions 5 Direct Access Diagnostics 2 Direct Import Marketing Co. 1

Direct Digital Imaging Technology (Beijing), Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Direct”