Contego Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Contego Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection, Paladin Carotid Post-dilation Balloon System with Integrated Embolic Protection (Paladin System)
2
Total
2
Cleared
0
Denied
Contego Medical, LLC has 2 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Contego Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qrac, LLC as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Contego Medical, LLC
2 devices