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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 10 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Sombrero Patella, Size 2, 10mm 5501.02.010
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.19.000
FDA UDI
Class IActive
Stem Trial 2015.10.170
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.012
FDA UDI
Class IIActive
36mm BIOLOX delta Femoral Head, 12/14 taper, -3.5mm Head Length 3203.36.035
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 56mm 3503.56.032
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.07.010
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.011
FDA UDI
Class IIActive
Platform Acetabular Cup with Ti-Coat 3401.48.000
FDA UDI
Class IIActive
22mm Femoral Head, 12/14 taper, +3.5mm offset 3200.22.350
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert with E-Link 3512.62.036
FDA UDI
Class IIActive
Stem Trial 2015.14.100
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.010
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.54.036
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.62.036
FDA UDI
Class IActive
Intramedullary Reamer 2014.13.000
FDA UDI
Class IActive
Augment Trial, Tibial 2902.05.010
FDA UDI
Class IActive
Universal Cone 6800.06.024
FDA UDI
Class IIActive
Femoral Trial 2108.03.000
FDA UDI
Class IActive
Platform Acetabular Cup Sizer 1225.44.000
FDA UDI
Class IActive
Narrow Distal Femur Cut Block SRI-10047
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6403.02.010
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.03.012
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2171.06.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.02.013
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 5, 12 mm, Final Packed, Sterile 5300.05.012
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 36mm Head, Size 62mm 3502.62.036
FDA UDI
Class IIActive
Patella Osteotomy Guide 2308.00.000
FDA UDI
Class IActive
22mm Femoral Head, 12/14 taper, +0mm offset 3200.22.000
FDA UDI
Class IIActive
Tibial Insert Trial 2205.02.016
FDA UDI
Class IActive
Stem Trial 2015.16.050
FDA UDI
Class IActive
36mm Femoral Head, 12/14 Taper, +7mm Offset 3200.36.700
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.018
FDA UDI
Class IIActive
Klassic Blade Femoral Stem, Porous, Size 4 3105.04.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.05.005
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2171.03.000
FDA UDI
Class IActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.04.000
FDA UDI
Class IActive
Klassic HD Neck Trial, Offset 1105.01.000
FDA UDI
Class IActive
Stem Trial 2015.13.100
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.46.028
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.03.018
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 52mm 3503.52.036
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.02.010
FDA UDI
Class IIActive
Femoral Cut Block, Pegless 2148.01.000
FDA UDI
Class IActive
Klassic Domed Patella with E-Link 5502.04.000
FDA UDI
Class IIActive
BiPolar Femoral Head Trial 1326.28.350
FDA UDI
Class IActive
Stem Trial 2015.12.170
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 5, 12 mm, Final Packed, Sterile 5301.05.012
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.020
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.016
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.