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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 34 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Tibial Insert, Ultra-PS, Size 5, 18 mm, Final Packed, Sterile 5301.05.018
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.10.050
FDA UDI
Class IIActive
Femoral Stem Adapter Wrench 2805.00.000
FDA UDI
Class IActive
Klassic Tibial Baseplate, Revision 6201.06.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.03.021
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.58.032
FDA UDI
Class IIActive
Klassic Blade Femoral Stem 3105.11.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.02.010
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.03.014
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.014
FDA UDI
Class IIActive
Hemispherical Acetabular Reamer 1207.49.000
FDA UDI
Class IActive
Tibial Stem Extension Reamer 2210.00.000
FDA UDI
Class IActive
Modular Tibial Broach, Klassic ONE 2237.05.000
FDA UDI
Class IActive
Klassic Femur, PS-Post 5101.05.000
FDA UDI
Class IIActive
Platform Acetabular Cup Sizer 1225.54.000
FDA UDI
Class IActive
Revision Tibial Baseplate Sizer and Trial 2903.03.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.56.032
FDA UDI
Class IIActive
Klassic Femur, PS-Post 5101.02.000
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.60.032
FDA UDI
Class IIActive
Klassic Tibial Augment & Screw 6405.03.010
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 5, 10 mm, Final Packed, Sterile 5301.05.010
FDA UDI
Class IIActive
Universal Cut Block, Klassic ONE 2158.00.000
FDA UDI
Class IActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.02.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.05.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.013
FDA UDI
Class IActive
Stem Trial 2015.17.200
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.022
FDA UDI
Class IIActive
Contoura Femoral Head Trial 1347.32.000
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.28.000
FDA UDI
Class IActive
Acetabular Insert Trial 1204.50.032
FDA UDI
Class IActive
32mm Femoral Head, 12/14 Taper, +0mm Offset 3200.32.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.016
FDA UDI
Class IIActive
Modular Distal Femoral Cut Guide Fixed 2149.00.006
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.20.040
FDA UDI
Class IIActive
Klassic Femoral Canal Finder, Modular 1345.00.000
FDA UDI
Class IActive
Klassic Blade Femoral Stem, Porous, Size 6 3105.06.000
FDA UDI
Class IIActive
Klassic Tibial Augment 6404.05.005
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.010
FDA UDI
Class IIActive
Klassic Tibial Baseplate with Ti-Coat, size 3 5202.03.000
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 54mm 3501.54.032
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.02.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.06.018
FDA UDI
Class IActive
Universal Cone Trial, Size 2, 12° 2022.02.012
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.02.010
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.62.032
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.014
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.012
FDA UDI
Class IIActive
Stem Trial 2015.14.200
FDA UDI
Class IActive
Universal Cone Reamer, Basket, Size 1-2, 12° 2020.01.012
FDA UDI
Class IActive
32mm BIOLOX delta Femoral Head, 12/14 taper, +7mm Head Length 3203.32.700
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.