Synovis Life Technologies. Inc. (A Subsidiary of Baxter is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synovis Life Technologies. Inc. (A Subsidiary of Baxter - FDA 510(k) ...
Recent clearances: PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology
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) Regulatory Record - Synovis Life Technologies. Inc. (A Subsidiary of Baxter
1 devices