Activortho, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Activortho, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ActivOrtho Continuous Compression Screw System, ActivOrtho Nitinol Compression Screw System
2
Total
2
Cleared
0
Denied
Activortho, Inc. has 2 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Activortho, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Backroads Consulting, Inc. and DuVal & Associates, P.A..
FDA 510(k) Regulatory Record - Activortho, Inc.
2 devices