Globus Sport and Health Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Globus Sport and Health Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: Diacare 7000
1
Total
1
Cleared
0
Denied
Globus Sport and Health Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Globus Sport and Health Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sigma Biomedical as regulatory consultant.
FDA 510(k) Regulatory Record - Globus Sport and Health Technologies, LLC
1 devices