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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 2 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.01.021
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.60.032
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 52mm 3503.52.032
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.56.028
FDA UDI
Class IActive
Universal Cone 6800.01.012
FDA UDI
Class IIActive
Acetabular X-Ray Templates 1212.00.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 4 , 16mm 5204.04.016
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 56mm 3501.56.032
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.03.010
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.47.028
FDA UDI
Class IActive
Klassic Femur, Nonporous 5105.01.000
FDA UDI
Class IIActive
Flexion/Extension Cut Block 2117.00.200
FDA UDI
Class IActive
Klassic Blade Femoral Stem 3105.12.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.011
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.01.018
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 48mm 3502.48.032
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.01.010
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 3 , 14mm 5204.03.014
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 1, 12 mm, Final Packed, Sterile 5300.01.012
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 60mm 3501.60.032
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 2, 14 mm, Final Packed, Sterile 5300.02.014
FDA UDI
Class IIActive
Universal Cone Reamer, Basket, Size 3-4, 18° 2020.03.018
FDA UDI
Class IActive
Patella Sizer/Clamp/Drill Guide, Klassic ONE, Tip 2311.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.022
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.20.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.012
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.016
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 56mm 3501.56.036
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.56.036
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.014
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.018
FDA UDI
Class IIActive
Revision Modular Tibial Broach 2905.03.000
FDA UDI
Class IActive
Stem Trial 2015.18.050
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.00.000
FDA UDI
Class IActive
Universal Cone 6800.02.012
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.024
FDA UDI
Class IIActive
Femur Trial 2147.04.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 3, 12 mm, Final Packed, Sterile 5300.03.012
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.46.032
FDA UDI
Class IIActive
Femoral Broach 1100.01.000
FDA UDI
Class IActive
Klassic Blade Femoral Stem, Porous, Size 9 3105.09.000
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 1 , 12mm 5204.01.012
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.06.014
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert Trial 1228.50.036
FDA UDI
Class IActive
3.2mm Drill Tip 1219.35.035
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.40.022
FDA UDI
Class IActive
Klassic Knee Femur, Size 6, Nonporous 5100.06.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 4, 14 mm, Final Packed, Sterile 5300.04.014
FDA UDI
Class IIActive
Tibial Insert Trial 2205.05.011
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.011
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.