FDA applicant
Kedumin Kits, Ltd.
FDA records 1 decision for Kedumin Kits, Ltd. (Rehovot, Israel, IL) in 1990: 1 510(k) clearance. All are in product code FHJ (Shield, Circumcision). 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 Kedumin Kits, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kedumin Kits, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kedumin Kits, Ltd.’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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