Syntr Health Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syntr Health Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SyntrFuge System
1
Total
1
Cleared
0
Denied
Syntr Health Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Syntr Health Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bqc Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Syntr Health Technologies, Inc.
1 devices