Ortho Development Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Development Corporation - FDA 510(k) Cleared Devices
Recent clearances: Balanced Knee® System TriMax PS Plus Tibial Insert, The Progen™ Trochanteric Nail System, Balanced Knee System Uni
14
Total
14
Cleared
0
Denied
Ortho Development Corporation has 14 FDA 510(k) cleared orthopedic devices. Based in Draper, US.
Last cleared in 2023. Active since 2015.
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 - Ortho Development Corporation
14 devices
Cleared
Oct 25, 2023
Balanced Knee® System TriMax PS Plus Tibial Insert
Orthopedic
29d
Cleared
Dec 21, 2021
The Progen™ Trochanteric Nail System
Orthopedic
253d
Cleared
Dec 16, 2021
Balanced Knee System Uni
Orthopedic
219d
Cleared
Jul 14, 2021
Pisces Spinal System
Orthopedic
285d
Cleared
Mar 31, 2020
The Gecko Spinal System
Orthopedic
56d
Cleared
Oct 31, 2018
Balanced Knee Revision System Trabecular Tibial Cone Augments
Orthopedic
90d
Cleared
Oct 12, 2018
BKS Revision Sleeves System
Orthopedic
120d
Cleared
Jun 20, 2018
Balanced Knee Revision System - Offset Junction Box
Orthopedic
90d
Cleared
May 30, 2018
Legend Acetabular Liners
Orthopedic
154d
Cleared
Aug 24, 2017
Entrada™ hip stem
Orthopedic
118d
Cleared
Mar 30, 2017
Ibis® Pedicle Screw System
Orthopedic
154d
Cleared
May 17, 2016
Escalade Legend Acetabular Shell
Orthopedic
29d
Cleared
Feb 18, 2016
Alpine Cemented Hip System
Orthopedic
105d
Cleared
Oct 27, 2015
Balanced Knee System TriMax CR Femoral Component and E-Vitalize CR and UC...
Orthopedic
84d