Amend Surgical, Inc. is one of 20445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amend Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 0.5cc NanoFUSE, 1.0cc NanoFUSE, 2cc NanoFUSE, 5cc NanoFUSE, 10cc NanoFUSE
1
Total
1
Cleared
0
Denied
Amend Surgical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Amend Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Simpson Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Amend Surgical, Inc.
1 devices