510(k) Report

FDA applicant

Central Plastic, Inc.

Eldorado, KS2 decisions1989–19910 recalls

FDA records 2 decisions for Central Plastic, Inc. (Eldorado, KS) from 1989 to 1991: 2 510(k) clearances. Most are in product codes EYF (Protector, Wound, Plastic) and FMK (Single Use Only Blood Lancet With An Integral…). 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 Central Plastic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Central Plastic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Central Plastic, 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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