Endo Vantage, LLC is one of 18966 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endo Vantage, LLC - FDA 510(k) Cleared Devices
Recent clearances: SurgicalPreview
1
Total
1
Cleared
0
Denied
Endo Vantage, LLC has 1 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Endo Vantage, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Endo Vantage, LLC
1 devices