Orthopaedic Implant Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthopaedic Implant Company - FDA 510(k) Cleared Devices
Recent clearances: OIC FLEX-FIX™ System, OIC Intramedullary Screw System, OIC Variable Angle Small Fragment Locking Plate System
10
Total
10
Cleared
0
Denied
Orthopaedic Implant Company has 10 FDA 510(k) cleared orthopedic devices. Based in Reno, US.
Latest FDA clearance: Feb 2024. Active since 2014.
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 - Orthopaedic Implant Company
10 devices
Cleared
Feb 02, 2024
OIC FLEX-FIX™ System
Orthopedic
92d
Cleared
Feb 13, 2023
OIC Intramedullary Screw System
Orthopedic
60d
Cleared
Jan 21, 2023
OIC Variable Angle Small Fragment Locking Plate System
Orthopedic
110d
Cleared
Apr 05, 2022
DRPx Locking Distal Radius Plate System
Orthopedic
231d
Cleared
May 06, 2021
DRPx Locking Distal Radius Plate System
Orthopedic
218d
Cleared
May 05, 2021
OIC External Fixation System
Orthopedic
21d
Cleared
Apr 08, 2019
OIC External Fixation System
Orthopedic
101d
Cleared
Sep 27, 2017
OIC External Fixation System
Orthopedic
155d
Cleared
Jul 09, 2015
OIC Intramedullary Nail System
Orthopedic
118d
Cleared
Jun 09, 2014
OIC VARIABLE ANGLE SMALL FRAGMENT LOCKING PLATE SYSTEM
Orthopedic
117d