FDA applicant
Medine Dynacor
FDA records 1 decision for Medine Dynacor (Walker, MI) in 1982: 1 510(k) clearance. All are in product code GBX (Catheter, Irrigation). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Medine Dynacor’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medine Dynacor since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medine Dynacor’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