Synergy Biomedical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synergy Biomedical - FDA 510(k) Cleared Devices
Recent clearances: BioSphere Putty, BioSphere Flex
2
Total
2
Cleared
0
Denied
Synergy Biomedical has 2 FDA 510(k) cleared medical devices. Based in Collegeville, US.
Latest FDA clearance: Dec 2024. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Synergy Biomedical Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Bruder Consulting & Venture Group.
FDA 510(k) Regulatory Record - Synergy Biomedical
2 devices