Medical Device Manufacturer · US , Flaggstaff , AZ

Geon Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Geon Corp. has 2 FDA 510(k) cleared medical devices. Based in Flaggstaff, US.

Historical record: 2 cleared submissions from 1996 to 2001. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Geon Corp. Filter by specialty or product code using the sidebar.

Geon Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Geon Corp.

2 devices

1-2 of 2