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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
—
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 32 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Tibial Stem Extension, 50mm 5600.00.050
FDA UDI
Class IIActive
Stem Trial 2015.18.150
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.28.035
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 1, 14 mm, Final Packed, Sterile 5301.01.014
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.013
FDA UDI
Class IActive
Offset Femoral Stem Trial Extractor 1317.00.000
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.28.000
FDA UDI
Class IIActive
Klassic Sombrero Patella with E-Link 5503.04.007
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.07.010
FDA UDI
Class IIActive
Tibial Sizer 2202.06.000
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.04.016
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.013
FDA UDI
Class IActive
Platform Acetabular Cup with Ti-Coat 3401.46.000
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.02.012
FDA UDI
Class IActive
Patella Sizer/Clamp/Drill Guide/Reamer, Klassic ONE, Handle 2310.00.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.01.011
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.45.000
FDA UDI
Class IActive
Femoral Cut Block 2106.01.000
FDA UDI
Class IActive
Platform Hooded Acetabular Insert with E-Link 3512.48.032
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.07.005
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.46.028
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 3 3103.03.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.03.013
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly, 5303.06.013
FDA UDI
Class IIActive
Klassic HD Modular Femoral Broach 1106.09.000
FDA UDI
Class IActive
Acetabular Cup Sizer 1200.50.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 2, 10 mm, Final Packed, Sterile 5300.02.010
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.014
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D, size 5 5102.05.000
FDA UDI
Class IIActive
Hooded Acetabular Insert Trial 1223.60.036
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.013
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.51.028
FDA UDI
Class IActive
Sombrero Patella Trial 2307.03.010
FDA UDI
Class IActive
Klassic Knee Femur, Revision 6100.07.000
FDA UDI
Class IIActive
Platform Acetabular Cup Sizer 1225.60.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.024
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.03.011
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.04.005
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 4, 16 mm, Final Packed, Sterile 5300.04.016
FDA UDI
Class IIActive
Femur/Patella Peg Drill 2114.00.000
FDA UDI
Class IActive
Augment Trial, Tibial 2902.03.005
FDA UDI
Class IActive
Platform Hooded Acetabular Insert with E-Link 3512.44.028
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.018
FDA UDI
Class IActive
All-Poly Tibial Broach Tower Assembly 2215.01.000
FDA UDI
Class IActive
Femoral Cut Block 2106.06.000
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.05.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.010
FDA UDI
Class IIActive
Hooded Acetabular Insert Trial 1223.64.036
FDA UDI
Class IActive
Tibial Insert Trial 2205.02.013
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.