FDA applicant
J.B.C and Co.
FDA records 2 decisions for J.B.C and Co. (Yorba Linda, CA) from 1998 to 2000: 2 510(k) clearances. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 J.B.C and Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for J.B.C and Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like J.B.C and 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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