Brm Extremities Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Brm Extremities Srl - FDA 510(k) Cleared Devices
Recent clearances: BRM Digitalis Spacer, BRM TOOL Screws
2
Total
2
Cleared
0
Denied
Brm Extremities Srl has 2 FDA 510(k) cleared medical devices. Based in Civate, IT.
Last cleared in 2023. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Brm Extremities Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Brm Extremities Srl
2 devices