Zefon Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zefon Intl. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Zefon Intl. has 2 FDA 510(k) cleared medical devices. Based in Ocala, US.
Historical record: 2 cleared submissions from 2008 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zefon Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zefon Intl.
2 devices