Synedgen, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Synedgen, Inc. has 3 FDA 510(k) cleared medical devices. Based in Claremont, US.
Historical record: 3 cleared submissions from 2015 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Synedgen, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Synedgen, Inc.
3 devices