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TOTAL JOINT ORTHOPEDICS, INC.

US

Last updated September 17, 2026

Information

Country
US
Address
1567 E. Stratford Avenue, Salt Lake City, UT, 84106
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3008544874
DUNS Number
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Catalogue (2063)

Page 30 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Domed Patella with E-Link 5502.03.000
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert Trial 1228.50.032
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.018
FDA UDI
Class IIActive
Klassic Sombrero Patella with E-Link 5503.03.010
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 1 , 12mm 5203.01.012
FDA UDI
Class IIActive
Tibial Insert Trial 2205.01.016
FDA UDI
Class IActive
Universal Cone 6800.03.018
FDA UDI
Class IIActive
Femoral Trial 2108.06.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.011
FDA UDI
Class IIActive
PS-Post Box Resection Guide 2172.02.000
FDA UDI
Class IActive
Distal Femoral Cut Guide Modular Base 2149.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.12.120
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.06.005
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.01.014
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem 3107.10.000
FDA UDI
Class IIActive
Tibial Insert Trial 2205.04.012
FDA UDI
Class IActive
Tibial Ream Guide, Klassic ONE 2235.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.011
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision 2126.03.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.018
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.52.032
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.014
FDA UDI
Class IIActive
Klassic ONE Knee PS-Post Auxiliary Instrumentation Tray 2412.00.000
FDA UDI
Class IActive
28mm Femoral Head, 12/14 taper, +3.5mm offset 3200.28.350
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 6 , 16mm 5204.06.016
FDA UDI
Class IIActive
Acetabular Shell with Ti-Coat, 48mm 3400.48.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.018
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.02.010
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.02.000
FDA UDI
Class IActive
Klassic BiPolar Sizing Handle, Locking 1341.28.000
FDA UDI
Class IActive
Stem Trial 2015.12.050
FDA UDI
Class IActive
Distal Femoral Augment Trial 2810.01.005
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.05.014
FDA UDI
Class IActive
Femoral Cut Block 2106.05.000
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.04.000
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.57.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.018
FDA UDI
Class IIActive
Fixed Distal Femoral Cut Guide, Klassic ONE 2156.00.005
FDA UDI
Class IActive
BiPolar Femoral Head Trial 1326.28.035
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.20.050
FDA UDI
Class IIActive
A/P Sizer, Klassic ONE 2161.00.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.02.016
FDA UDI
Class IActive
Tibial Alignment Guide, Lower Tower SSI-10029
FDA UDI
Class IActive
Stem Trial 2015.14.050
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.06.012
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.05.021
FDA UDI
Class IIActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.28.035
FDA UDI
Class IIActive
Klassic Sombrero Patella with E-Link 5503.01.010
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.013
FDA UDI
Class IIActive
Patella Clamp 2304.00.000
FDA UDI
Class IActive

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Sep 23, 2025Z-0432-2026—open, classified

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.