G-Surg GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
G-Surg GmbH - FDA 510(k) Cleared Devices
Recent clearances: GERDX-System
1
Total
1
Cleared
0
Denied
G-Surg GmbH has 1 FDA 510(k) cleared medical devices. Based in Seeon-Seebruck, DE.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by G-Surg GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novineon CRO GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - G-Surg GmbH
1 devices