Oystershell NV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Oystershell NV - FDA 510(k) Cleared Devices
Recent clearances: Pixie Skin Tag
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) Regulatory Record - Oystershell NV
1 devices