Gordian Surgical, Ltd. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Gordian Surgical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TroClose 1200, TroClose1200, TroClose1200 Cannula, TroClose1200
3
Total
3
Cleared
0
Denied
Gordian Surgical, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Karmiel, IL.
Latest FDA clearance: Dec 2025. Active since 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gordian Surgical, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Dr. Susan Alpert and Avio Medtech Consulting.
FDA 510(k) Regulatory Record - Gordian Surgical, Ltd.
3 devices