FDA applicant
Ferris Mfg. Corp.
FDA records 20 decisions for Ferris Mfg. Corp. (Burr Ridge, IL) from 1978 to 2005: 20 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and FRO (Dressing, Wound, Drug). 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 Ferris Mfg. Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ferris Mfg. Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ferris Mfg. 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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