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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 37 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.014
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.021
FDA UDI
Class IIActive
Calcar Planer 1327.50.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.14.150
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2170.07.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.20.120
FDA UDI
Class IIActive
Stem Trial 2015.15.050
FDA UDI
Class IActive
Klassic Sombrero Patella with E-Link 5503.04.010
FDA UDI
Class IIActive
Tibial Insert Trial 2205.06.011
FDA UDI
Class IActive
Klassic HD Hip Case 3, Femoral Preparation Instruments 1403.00.000
FDA UDI
Class IActive
Angel Wing, Klassic ONE 2163.00.000
FDA UDI
Class IActive
Stem Trial 2015.11.150
FDA UDI
Class IActive
Patella Planer 2305.31.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.011
FDA UDI
Class IIActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.06.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.018
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.03.000
FDA UDI
Class IActive
Stem Trial 2015.20.170
FDA UDI
Class IActive
Modular Knee Impactor Head, Tibia 2227.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.020
FDA UDI
Class IIActive
Klassic HD Hip Offset Femoral Stem Trial 1316.01.000
FDA UDI
Class IActive
Stem Trial 2015.15.070
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.10.200
FDA UDI
Class IIActive
Klassic HD Neck Trial, Offset 1105.02.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.02.013
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 6, 10 mm, Final Packed, Sterile 5301.06.010
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.22.400
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.43.022
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.06.011
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.05.010
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.016
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.15.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.02.016
FDA UDI
Class IIActive
Cancellous Bone Screw with 6.5mm Head Diameter, 20mm 3600.20.065
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.018
FDA UDI
Class IIActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.04.000
FDA UDI
Class IActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.06.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.011
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 3 , 14mm 5203.03.014
FDA UDI
Class IIActive
Platform Acetabular Cup Sizer 1225.48.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.02.018
FDA UDI
Class IIActive
Contoura Femoral Head Trial 1347.36.035
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.02.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.01.014
FDA UDI
Class IActive
Klassic Knee Case 3, Patella/Misc. Preparation Instrumentation 2407.00.000
FDA UDI
Class IActive
Stem Trial 2015.20.150
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.06.013
FDA UDI
Class IIActive
OrthoGroup Straight Broach Holder 1120.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.011
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.05.000
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.