510(k) Report

FDA applicant

The Bfgoodrich Co.

Brecksville, OH4 decisions1987–19880 recalls

FDA records 4 decisions for The Bfgoodrich Co. (Brecksville, OH) from 1987 to 1988: 4 510(k) clearances. All are in product code NAD (Dressing, Wound, Occlusive). 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 Bfgoodrich Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Bfgoodrich Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Bfgoodrich Co.’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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