Ezono AG is one of 491 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Ezono AG has 1 FDA 510(k) cleared medical devices. Based in Jena, DE.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ezono AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ezono AG
1 devices