510(k) Report

FDA applicant

Creative Research and Mfg., Inc.

Mchenry, IL2 decisions1981–19820 recalls

FDA records 2 decisions for Creative Research and Mfg., Inc. (Mchenry, IL) from 1981 to 1982: 2 510(k) clearances. All are in product code GAA (Needle, Aspiration And Injection, Disposable). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Creative Research and Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Creative Research and Mfg., 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.