FDA applicant

Radiographic Digital Imaging, Inc.

Compton, CA3 decisions1995–20020 recalls

FDA records 3 decisions for Radiographic Digital Imaging, Inc. (Compton, CA) from 1995 to 2002: 3 510(k) clearances. Most are in product codes LMA (Digitizer, Image, Radiological) and LLZ (System, Image Processing, Radiological). Its devices cite 1 predicate, 1 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 Radiographic Digital Imaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Radiographic Digital Imaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Radiographic Digital Imaging, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Radiographic Digital Imaging, Inc.

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?