510(k) Report

FDA applicant

Creative Design Systems, Inc.

Carlstadt, NJ1 decision1991–19910 recalls

FDA records 1 decision for Creative Design Systems, Inc. (Carlstadt, NJ) in 1991: 1 510(k) clearance. All are in product code GYB (Media, Electroconductive). 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, neurology panel, where it files most

How often FDA has decided Creative Design Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Creative Design Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Creative Design Systems, Inc.’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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Other applicant names beginning “Creative”

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