FDA applicant
Kenex, Ltd.
FDA records 4 decisions for Kenex, Ltd. (England, GB) in 1995: 4 510(k) clearances. Most are in product codes KPY (Shield, Protective, Personnel) and IXA (Cassette, Radiographic Film). 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 Kenex, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kenex, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kenex, 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