FDA applicant
Kaycor Intl., Ltd.
FDA records 7 decisions for Kaycor Intl., Ltd. (Mchenry, IL) from 1981 to 1997: 7 510(k) clearances. Most are in product codes EKX (Handpiece, Direct Drive, Ac-Powered) and KLC (Chair, Dental, With Operative Unit). Its devices cite 1 predicate, 1 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 Kaycor Intl., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kaycor Intl., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kaycor Intl., 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