FDA applicant
Furlong Industries
FDA records 1 decision for Furlong Industries (Grayslake, IL) in 1999: 1 510(k) clearance. All are in product code 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 Furlong Industries’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Furlong Industries since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Furlong Industries’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report