Medical Device Manufacturer · US , Fr. Myers , FL

Flospine - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Flospine has 4 FDA 510(k) cleared medical devices. Based in Fr. Myers, US.

Last cleared in 2023. Active since 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Flospine Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.

Flospine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Flospine

4 devices

1-4 of 4