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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 4 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Femur, Revision 6100.01.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.010
FDA UDI
Class IIActive
Femoral Head Remover 1331.00.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.01.014
FDA UDI
Class IActive
Femoral Head Trial 1306.32.350
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.10.100
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.46.022
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.06.010
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.010
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.56.036
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 2, 18 mm, Final Packed, Sterile 5300.02.018
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.05.013
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 6, 12 mm, Final Packed, Sterile 5301.06.012
FDA UDI
Class IIActive
Tibial Stem Extension Reamer 2209.00.125
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.010
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 3 , 10mm 5204.03.010
FDA UDI
Class IIActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 7 3101.07.000
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 9 3103.09.000
FDA UDI
Class IIActive
Tibial Insert Trial 2205.06.018
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.021
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.32.105
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.013
FDA UDI
Class IIActive
Tibial Baseplate Trial, Flat 2204.03.100
FDA UDI
Class IActive
All-Poly Tibial Broach Tower Assembly 2215.03.000
FDA UDI
Class IActive
Tibial Alignment Guide, Upper Tower, Klassic ONE 2249.00.000
FDA UDI
Class IActive
Klassic Sombrero Patella with E-Link 5503.02.007
FDA UDI
Class IIActive
36mm BIOLOX delta Femoral Head, 12/14 taper, +7mm Head Length 3203.36.700
FDA UDI
Class IIActive
Acetabular Cup Sizer 1200.48.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.62.036
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.03.016
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 60mm 3503.60.032
FDA UDI
Class IIActive
Klassic HD Hip Case 1, Miscellaneous Hip Instruments 1401.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.012
FDA UDI
Class IIActive
Distal Femoral Cut Guide, Fixed 2140.00.004
FDA UDI
Class IActive
PS-Post Box Trial, Klassic ONE 2171.02.000
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6402.02.010
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.010
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem, Porous, Size 2 3107.02.000
FDA UDI
Class IIActive
OrthoGroup Double Offset Broach Holder, Left 1118.00.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.52.028
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.52.036
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.012
FDA UDI
Class IIActive
Bone Awl 1211.00.000
FDA UDI
Class IActive
Stem Trial 2015.15.200
FDA UDI
Class IActive
Stem Trial 2015.12.070
FDA UDI
Class IActive
Intramedullary Reamer 2014.19.000
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 4, 7mm 5501.04.007
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.62.036
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.47.028
FDA UDI
Class IActive
Universal Cone Trial, Size 5, 24° 2022.05.024
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.