Restor3d is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Restor3d - FDA 510(k) Cleared Devices
Recent clearances: Veritas Reverse Total Shoulder System, Kinos Total Ankle System, restor3d Reverse Total Shoulder Arthroplasty System
12
Total
12
Cleared
0
Denied
Restor3d has 12 FDA 510(k) cleared orthopedic devices. Based in Durham, US.
Latest FDA clearance: May 2026. Active since 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Restor3d
12 devices
Cleared
May 07, 2026
Veritas Reverse Total Shoulder System
Orthopedic
146d
Cleared
Sep 03, 2025
Kinos Total Ankle System
Orthopedic
30d
Cleared
May 19, 2025
restor3d Reverse Total Shoulder Arthroplasty System
Orthopedic
174d
Cleared
Oct 18, 2024
Kinos Total Ankle System
Orthopedic
28d
Cleared
Jul 22, 2024
Kinos Total Ankle System
Orthopedic
59d
Cleared
Jan 22, 2024
restor3d TIDAL Lumbar Interbody Fusion System
Orthopedic
31d
Cleared
Nov 28, 2023
Kinos Axiom Total Ankle System
Orthopedic
95d
Cleared
Aug 03, 2023
Extremity Staple
Orthopedic
76d
Cleared
Mar 30, 2023
Axiom PSR System
Orthopedic
150d
Cleared
Jun 17, 2022
restor3d TiDAL Lumbar Interbody Fusion Device
Orthopedic
114d
Cleared
Jan 04, 2022
restor3d Pin Implants
Orthopedic
208d
Cleared
Mar 19, 2020
restor3d Metallic Interference Screw
Orthopedic
93d