Global Biomedica s.r.o. - FDA 510(k) Cleared Devices
Recent clearances: BMD Titanium Spinal Fusion System
1
Total
1
Cleared
0
Denied
Global Biomedica s.r.o. has 1 FDA 510(k) cleared medical devices. Based in Ceský Tešín, CZ.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Global Biomedica s.r.o. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Global Biomedica s.r.o.
1 devices