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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 5 of 42
DeviceModel / ReferenceRegistriesClassStatus
Stem Trial 2015.15.120
FDA UDI
Class IActive
Modular Femoral Head Trial 1326.32.700
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.43.022
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6403.04.005
FDA UDI
Class IIActive
Pin Driver, 2.25mm Square 2008.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.011
FDA UDI
Class IIActive
Femoral Cut Block, Pegless 2148.04.000
FDA UDI
Class IActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.04.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.05.012
FDA UDI
Class IActive
Augment Trial, Tibial 2902.03.010
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 6 , 14mm 5203.06.014
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 3 , 12mm 5203.03.012
FDA UDI
Class IIActive
Hooded Acetabular Insert Trial 1223.44.028
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.016
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 1, 12 mm, Final Packed, Sterile 5301.01.012
FDA UDI
Class IIActive
Klassic HD Modular Femoral Broach 1106.07.000
FDA UDI
Class IActive
Platform Acetabular Cup Sizer 1225.46.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.012
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6402.02.005
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.021
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.010
FDA UDI
Class IActive
Augment Trial, Tibial 2902.01.010
FDA UDI
Class IActive
Stem Trial 2015.12.100
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem, Porous, Size 1 3107.01.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.03.014
FDA UDI
Class IActive
Femur Trial 2147.03.000
FDA UDI
Class IActive
Klassic Knee Case 1, Femoral Preparation Instrumentation 2401.00.000
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.01.000
FDA UDI
Class IActive
Drill and Pin Set, Screw 2705.00.000
FDA UDI
Class IActive
Femur/Tibia Implant Impactor Handle 2110.00.000
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.36.035
FDA UDI
Class IIActive
A/P Sizer 2105.00.000
FDA UDI
Class IActive
Platform Neutral Acetabular Insert with E-Link 3511.44.028
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.022
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.016
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.011
FDA UDI
Class IIActive
22mm BIOLOX delta Ceramic Femoral Head, 12/14 taper 3203.22.400
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.010
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 62mm 3501.62.032
FDA UDI
Class IIActive
A/P Sizer, Pegless 2105.00.100
FDA UDI
Class IActive
Canal Finder Reamer 1300.00.000
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.64.032
FDA UDI
Class IActive
Sombrero Patella Trial 2307.05.010
FDA UDI
Class IActive
Acetabular Insert Trial 1204.56.036
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.011
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.021
FDA UDI
Class IIActive
Platform Acetabular Cup Sizer 1225.62.000
FDA UDI
Class IActive
Femur Extractor/Impactor Head 2109.00.100
FDA UDI
Class IActive
Modular Liner Impactor Head 1222.36.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.20.150
FDA UDI
Class IIActive

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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.