Medical Device Manufacturer · BE , Merelbeke

Oystershell NV - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Oystershell NV has 1 FDA 510(k) cleared medical devices. Based in Merelbeke, BE.

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

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

FDA 510(k) cleared devices by Oystershell NV

1 devices
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