Medical Device Manufacturer · US , Dana Point , CA

Sapphire Medical Group - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017
4
Total
4
Cleared
0
Denied

Sapphire Medical Group has 4 FDA 510(k) cleared medical devices. Based in Dana Point, US.

Latest FDA clearance: Mar 2024. Active since 2017. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Sapphire Medical Group Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Sapphire Medical Group

4 devices
1-4 of 4
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All4 Orthopedic 4