Ortho Development Corp. - FDA 510(k) Cleared Devices
Recent clearances: Balanced Knee System TriMax Porous Femoral Components, Trivicta® Hip Stem, BKS Revision System
45
Total
43
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ortho Development Corp. Orthopedic ✕
42 devices
Cleared
Dec 19, 2025
Balanced Knee System TriMax Porous Femoral Components
Orthopedic
84d
Cleared
May 22, 2025
Trivicta® Hip Stem
Orthopedic
49d
Cleared
Oct 25, 2024
BKS Revision System
Orthopedic
29d
Cleared
Oct 11, 2024
Legend® Acetabular Shell
Orthopedic
22d
Cleared
Mar 08, 2024
Trivicta™ Hip Stem
Orthopedic
105d
Cleared
Dec 11, 2014
IBIS PEDICLE SCREW SYSTEM
Orthopedic
128d
Cleared
Jun 20, 2014
ENCOMPASS 10/12 HIP STEM
Orthopedic
295d
Cleared
Mar 11, 2014
OVATION TRIBUTE HIP STEM
Orthopedic
126d
Cleared
Feb 18, 2014
KASM KNEE ARTICULATING SPACER MOLDS
Orthopedic
98d
Cleared
Oct 16, 2013
OVATION 10/12 HIP STEM
Orthopedic
187d
Cleared
Oct 11, 2013
BALANCED KNEE SYSTEM HIGH FLEX VITAMIN E PS TIBIAL INSERT AND PATELLA
Orthopedic
155d
Cleared
Aug 20, 2013
PAGODA PEDICLE SCREW SYSTEM
Orthopedic
63d
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