Synchro Medical is one of 18461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synchro Medical - FDA 510(k) Cleared Devices
Recent clearances: Synchro-Medical TIGER TRACK Screw System, TOEGRIP, IMPLANT FOR PROXIMAL INTER-PHALANGEAL ARTHRODESIS
2
Total
2
Cleared
0
Denied
Synchro Medical has 2 FDA 510(k) cleared medical devices. Based in West Lawn, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Synchro Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mark F Schenk Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Synchro Medical
2 devices