Jomed AG is one of 16313 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jomed AG - FDA 510(k) Cleared Devices
Recent clearances: JOSTENT SELFX, MODELS 015SX4406, MODIFICATION TO FOX PTA CATHETER, FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, A14007, A14008
3
Total
3
Cleared
0
Denied
Jomed AG has 3 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 3 cleared submissions from 2001 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Jomed AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jomed AG
3 devices