Synovis Life Technologies. Inc. (A Subsidiary of Baxter - FDA 510(k) ...
1
Total
1
Cleared
0
Denied
Synovis Life Technologies. Inc. (A Subsidiary of Baxter has 1 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Synovis Life Technologies. Inc. (A Subsidiary of Baxter Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Synovis Life Technologies. Inc. (A...
1 devices