In2bones USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In2bones USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: CoLink® & CoLag® Non-Sterile Screws, NeoSpan® Compression Implant System, IBS-B MIS Beveled Screw System
26
Total
26
Cleared
0
Denied
In2bones USA, LLC has 26 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Latest FDA clearance: May 2026. Active since 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mrc-X, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - In2bones USA, LLC
26 devices
Cleared
May 30, 2026
CoLink® & CoLag® Non-Sterile Screws
Orthopedic
52d
Cleared
May 24, 2024
NeoSpan® Compression Implant System
Orthopedic
241d
Cleared
Jul 27, 2023
IBS-B MIS Beveled Screw System
Orthopedic
90d
Cleared
May 27, 2022
CoLink PCR Plating System
Orthopedic
185d
Cleared
Mar 31, 2022
Hercules Syndesmosis Implant System
Orthopedic
59d
Cleared
Dec 17, 2021
Avenger Radial Head System
Orthopedic
99d
Cleared
Dec 13, 2021
CoLink NeoFuse Plating System
Orthopedic
81d
Cleared
Nov 18, 2021
CoLink Vallux Plating System
Orthopedic
101d
Cleared
May 04, 2021
CoLink Sfx Implant System
Orthopedic
137d
Cleared
Mar 12, 2021
CoLink Mfx Implant System
Orthopedic
60d
Cleared
Aug 20, 2020
Hercules Suture Anchor System
Orthopedic
65d
Cleared
Jul 15, 2020
CoLink Plating System
Orthopedic
77d