Intravent Medical Partners is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intravent Medical Partners - FDA 510(k) Cleared Devices
Recent clearances: SOLOPASS 2.0 System
1
Total
1
Cleared
0
Denied
Intravent Medical Partners has 1 FDA 510(k) cleared medical devices. Based in Blue Bell, US.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Intravent Medical Partners Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProPharma MedTech as regulatory consultant.
FDA 510(k) Regulatory Record - Intravent Medical Partners
1 devices