Flospine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Flospine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Largo PEEK Interbody System
1
Total
1
Cleared
0
Denied
Flospine, LLC has 1 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Flospine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Flospine, LLC
1 devices