Geon Corporation - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Geon Corporation has 3 FDA 510(k) cleared medical devices. Based in Flagstaff, US.
Latest FDA clearance: Feb 2025. Active since 2010. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Geon Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alfabeta Clinical Research Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Geon Corporation
3 devices