Restor3D, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Restor3D, Inc. has 6 FDA 510(k) cleared medical devices. Based in Durham, US.
Latest FDA clearance: Dec 2025. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Restor3D, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Restor3D, Inc.
6 devices
Cleared
Dec 05, 2025
Velora Acetabular System
Orthopedic
157d
Cleared
Mar 27, 2025
iTotal® Identity™ Cruciate Retaining 3DP Porous Knee Replacement System
Orthopedic
111d
Cleared
Mar 24, 2025
TIDAL Fusion Cage System
Orthopedic
228d
Cleared
Apr 29, 2024
restor3d Kinos Axiom Total Ankle System
Orthopedic
59d
Cleared
May 25, 2022
restor3d MTP Implant
Orthopedic
728d
Cleared
Jun 17, 2021
Restor3d Utility Wedge
Orthopedic
395d