Medical Device Manufacturer · US , Fr. Myers , FL

Flospine - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014
4
Total
4
Cleared
0
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.

FDA 510(k) Regulatory Record - Flospine
4 devices
1-4 of 4
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All4 Orthopedic 4