Relievant Medsystems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Relievant Medsystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Intracept Intraosseous Nerve Ablation System, Intracept Intraosseous Nerve Ablation System
4
Total
4
Cleared
0
Denied
Relievant Medsystems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Hayward, US.
Last cleared in 2022. Active since 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Relievant Medsystems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Relievant Medsystems, Inc.
4 devices
Cleared
Oct 26, 2022
Intracept Intraosseous Nerve Ablation System
Neurology
89d
Cleared
Mar 11, 2022
Intracept Intraosseous Nerve Ablation System
Neurology
92d
Cleared
Jan 22, 2009
INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS:...
General & Plastic Surgery
29d
Cleared
Oct 05, 2007
INTRACEPT BI-POLAR RF PROBE, MODEL 04814
General & Plastic Surgery
232d