Medical Device Manufacturer · IT , Civate

Brm Extremities Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
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
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