Medical Device Manufacturer · US , Durham , NC

Restor3D, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2021

Recent clearances: Velora Acetabular System, iTotal® Identity™ Cruciate Retaining 3DP Porous Knee Replacement System, TIDAL Fusion Cage System

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) Regulatory Record - Restor3D, Inc.

6 devices
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