FDA applicant
G.B.F. Industries, Inc.
FDA records 5 decisions for G.B.F. Industries, Inc. (New York, NY) from 1985 to 1987: 5 510(k) clearances. Most are in product codes JJY (Multi-Analyte Controls, All Kinds (Assayed)) and EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided G.B.F. Industries, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for G.B.F. Industries, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like G.B.F. Industries, 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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