Rivarp Medical Private Limited is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Rivarp Medical Private Limited - FDA 510(k) Cleared Devices
Recent clearances: Kentrospine PSS Pedicle Screw System
1
Total
1
Cleared
0
Denied
Rivarp Medical Private Limited has 1 FDA 510(k) cleared medical devices. Based in Bangalore, IN.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rivarp Medical Private Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rivarp Medical Private Limited
1 devices