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.
1 devices