Celon AG Medical Instruments is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Celon AG Medical Instruments - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Celon AG Medical Instruments has 2 FDA 510(k) cleared medical devices. Based in Teltow, DE.
Historical record: 2 cleared submissions from 2003 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Celon AG Medical Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Celon AG Medical Instruments
2 devices