Medical Device Manufacturer · US , Chicago , IL

Cypris Medical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied

Cypris Medical has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.

Latest FDA clearance: May 2024. Active since 2024. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Cypris Medical

2 devices
1-2 of 2
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