Cardo Medical, Inc. is one of 20558 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardo Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDO MEDICAL FEMORAL CEMENT RESTRICTOR, MODEL 503-MCRX, CARDO MEDICAL CERAMIC HIP SYSTEM
2
Total
2
Cleared
0
Denied
Cardo Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Clifton, US.
Historical record: 2 cleared submissions from 2010 to 2010. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cardo Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardo Medical, Inc.
2 devices