Medical Device Manufacturer · US , Carmel , IN

Redpoint Medical, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Redpoint Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Carmel, US.

Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Redpoint Medical, LLC 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 - Redpoint Medical, LLC
1 devices
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