Geon Corporation is one of 16449 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Geon Corporation - FDA 510(k) Cleared Devices
Recent clearances: Geon (S2) Nasal Aspirator, Geonic Nasal Aspirator, Geonic Nasal Cleaner, GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FA
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