Baxter/ Synovis Micro Companies Alliance, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baxter/ Synovis Micro Companies Alliance, Inc. - FDA 510(k) Cleared D...
Recent clearances: Gem FlowCoupler System, Gem FlowCoupler System
2
Total
2
Cleared
0
Denied
Baxter/ Synovis Micro Companies Alliance, Inc. has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Baxter/ Synovis Micro Companies Alliance, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baxter/ Synovis Micro Companies Alliance, Inc.
2 devices