FDA applicant

Dynamic Digital Displays, Inc.

Philadelphia, PA1 decision1988–19881 recall

FDA records 1 decision for Dynamic Digital Displays, Inc. (Philadelphia, PA) in 1988: 1 510(k) clearance. All are in product code JAK (System, X-Ray, Tomography, Computed). 1 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 Dynamic Digital Displays, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynamic Digital Displays, Inc. since 2007.

Recalls per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Dynamic”

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

Dynamic Technology Corp. 4 Dynamic Imaging, Inc. 3 Dynamic Systems, Inc. 2 Dynamic Marketing Ent. 1 Dynamic Air, Inc. 1 Dynamic Functional Positioner, Inc. 1 Dynamic Innovations, Inc. 1 Dynamic Plantations Sdn Bhd 1 Dynamic Healthcare Technologies, Inc. 1

Dynamic Digital Displays, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Dynamic”