Anjon Holdings, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anjon Holdings, LLC - FDA 510(k) Cleared Devices
Recent clearances: Anjon Bremer Halo System, Anjon Bremer Halo System
2
Total
2
Cleared
0
Denied
Anjon Holdings, LLC has 2 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Anjon Holdings, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Anjon Holdings, LLC
2 devices