FDA applicant

The Buckeye Cellulose Corp.

Mchenry, IL18 decisions1980–19830 recalls

FDA records 18 decisions for The Buckeye Cellulose Corp. (Mchenry, IL) from 1980 to 1983: 18 510(k) clearances. Most are in product codes FYA (Gown, Surgical) and KKX (Drape, Surgical, Antimicrobial). 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 The Buckeye Cellulose Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Buckeye Cellulose Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Buckeye Cellulose Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Buckeye Cellulose Corp.’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 “The”

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

Buckeye Medical Technologies, LLC 1

The Buckeye Cellulose Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”