Forge Medical, Inc. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Forge Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VasoStat Hemostasis Device, VASOSTAT HEMOSTASIS DEVICE
2
Total
2
Cleared
0
Denied
Forge Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Wayne, US.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Forge Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Texel Fortis, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Forge Medical, Inc.
2 devices