Brm Extremities is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brm Extremities - FDA 510(k) Cleared Devices
Recent clearances: BRM TOOL Screws, BIOPLAN Subtalar Implant, NewPrim System
2
Total
2
Cleared
0
Denied
Brm Extremities has 2 FDA 510(k) cleared medical devices. Based in Milano, US.
Last cleared in 2022. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Brm Extremities 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
2 devices