Rinovum Subsidiary 2, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rinovum Subsidiary 2, LLC - FDA 510(k) Cleared Devices
Recent clearances: Revive Reusable Bladder Support
1
Total
1
Cleared
0
Denied
Rinovum Subsidiary 2, LLC has 1 FDA 510(k) cleared medical devices. Based in Monroeville, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Rinovum Subsidiary 2, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Rinovum Subsidiary 2, LLC
1 devices