Synergy Biomedical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synergy Biomedical, LLC - FDA 510(k) Cleared Devices
Recent clearances: BioSphere MIS Putty (BioSphere MIS)
2
Total
2
Cleared
0
Denied
Synergy Biomedical, LLC has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 2013 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Synergy Biomedical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Synergy Biomedical, LLC
2 devices