Surgvision GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Surgvision GmbH - FDA 510(k) Cleared Devices
Recent clearances: EXPLORER AIR® II (8001, 8002, 8003), EXPLORER AIR® II, Explorer Air II
3
Total
3
Cleared
0
Denied
Surgvision GmbH has 3 FDA 510(k) cleared medical devices. Based in Munich, DE.
Latest FDA clearance: Mar 2024. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgvision GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgvision GmbH
3 devices