FDA applicant
Nagor, Ltd.
FDA records 2 decisions for Nagor, Ltd. (British Isles, VG) from 1998 to 1999: 2 510(k) clearances. All are in product code MDA (Elastomer, Silicone, For Scar Management). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Nagor, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Nagor, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Nagor, Ltd.’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