Gyder Surgical Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Gyder Surgical Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: GYDER® Hip System
1
Total
1
Cleared
0
Denied
Gyder Surgical Pty, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Mulgrave, AU.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Gyder Surgical Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Global Strategic Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Gyder Surgical Pty, Ltd.
1 devices