Bespa Global, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bespa Global, LLC - FDA 510(k) Cleared Devices
Recent clearances: BESPA Charcot System
1
Total
1
Cleared
0
Denied
Bespa Global, LLC has 1 FDA 510(k) cleared medical devices. Based in Cape Elizabeth, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bespa Global, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bespa Global, LLC
1 devices