FDA applicant
Broadline Medical Industries
FDA records 2 decisions for Broadline Medical Industries (Inverness, IL) in 1999: 2 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) 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
How often FDA has decided Broadline Medical Industries’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Broadline Medical Industries since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Broadline Medical Industries’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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