Relign Corporation, Subsidiary of Zimmer Biomet is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Relign Corporation, Subsidiary of Zimmer Biomet - FDA 510(k) Cleared ...
Recent clearances: Tricera Arthroscopic System
1
Total
1
Cleared
0
Denied
Relign Corporation, Subsidiary of Zimmer Biomet has 1 FDA 510(k) cleared medical devices. Based in Campbell, US.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Relign Corporation, Subsidiary of Zimmer Biomet Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Relign Corporation, Subsidiary of Zimmer Biomet
1 devices