Synovis Life Technologies, Inc. (Baxter International Inc.) 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. (Baxter International Inc.) - FDA 510...
Recent clearances: Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)
1
Total
1
Cleared
0
Denied
Synovis Life Technologies, Inc. (Baxter International Inc.) has 1 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Synovis Life Technologies, Inc. (Baxter International Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synovis Life Technologies, Inc. (Baxter International Inc.)
1 devices