Total Joint Orthopedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Total Joint Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Platform® Acetabular System, Klassic Knee System, Klassic Knee System
22
Total
22
Cleared
0
Denied
Total Joint Orthopedics, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Sunnyvale, US.
Latest FDA clearance: Jul 2026. Active since 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and Macra, LLC.
FDA 510(k) Regulatory Record - Total Joint Orthopedics, Inc.
22 devices
Cleared
Jul 23, 2026
Klassic Infection Spacer System
Orthopedic
58d
Cleared
Sep 23, 2022
Platform® Acetabular System
Orthopedic
217d
Cleared
Jun 22, 2022
Klassic Knee System
Orthopedic
370d
Cleared
Jul 23, 2021
Klassic Knee System
Orthopedic
60d
Cleared
Oct 09, 2020
Klassic Knee System Tibial Inserts, PS-Max
Orthopedic
21d
Cleared
Mar 29, 2019
Klassic Knee System - Klassic Knee PS-Post Femur
Orthopedic
98d
Cleared
Mar 15, 2019
Klassic Knee System - Sombrero Patella with Standard Poly, Klassic Knee...
Orthopedic
35d
Cleared
May 09, 2018
Klassic HD® Hip System
Orthopedic
30d
Cleared
Mar 09, 2018
Klassic® Knee System
Orthopedic
49d
Cleared
Oct 27, 2017
Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low...
Orthopedic
28d
Cleared
Oct 28, 2016
Klassic Knee System
Orthopedic
59d
Cleared
Oct 27, 2016
Klassic Femur, Porous, Klassic Tibial Baseplate, Porous
Orthopedic
77d