Rivarp Medical Pvt., Ltd. is one of 126 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Rivarp Medical Pvt., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Kentrospine Viktr-MIS® Pedicle screw system
1
Total
1
Cleared
0
Denied
Rivarp Medical Pvt., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Bangalore, IN.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rivarp Medical Pvt., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rivarp Medical Pvt., Ltd.
1 devices