FDA applicant
Conkin Surgical Instruments, Ltd.
FDA records 1 decision for Conkin Surgical Instruments, Ltd. (Toronta, Ontario, CA) in 1998: 1 510(k) clearance. All are in product code HDP (Elevator, Uterine). 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 Conkin Surgical Instruments, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Conkin Surgical Instruments, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Conkin Surgical Instruments, 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