Sapphire Medical Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sapphire Medical Group - FDA 510(k) Cleared Devices
Recent clearances: MATRIX HA PEEK Cervical IBF System, Matrix HA PEEK Cervical Implant System, SMG Anterior Cervical Plate System
4
Total
4
Cleared
0
Denied
Sapphire Medical Group has 4 FDA 510(k) cleared medical devices. Based in Dana Point, US.
Latest FDA clearance: Mar 2024. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sapphire Medical Group Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Consultant and Innovasis, Inc..
FDA 510(k) Regulatory Record - Sapphire Medical Group
4 devices