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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 21 of 42
DeviceModel / ReferenceRegistriesClassStatus
Tibial Baseplate Trial, Pegless 2204.05.200
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.05.010
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.016
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.44.028
FDA UDI
Class IIActive
Acetabular Cup Sizer 1200.56.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 5, 16 mm, Final Packed, Sterile 5301.05.016
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.021
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 2 , 10mm 5204.02.010
FDA UDI
Class IIActive
Tibial Baseplate Trial, Flat 2204.05.100
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.46.000
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem 3107.12.000
FDA UDI
Class IIActive
Femoral Neck Osteotomy Ruler 1302.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.03.018
FDA UDI
Class IActive
Stem Trial 2015.11.070
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.010
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.05.012
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 2, 12 mm, Final Packed, Sterile 5301.02.012
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.13.000
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.64.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.06.013
FDA UDI
Class IActive
Universal Cone Impactor Head, Size 6, 24° 2021.06.024
FDA UDI
Class IActive
Distal Hip Reamer, Sz 10 1349.10.000
FDA UDI
Class IActive
Quick Pin, Long Smooth 2004.50.100
FDA UDI
Class IActive
Klassic Femur, PS-Post 5101.04.000
FDA UDI
Class IIActive
Modular Tibial Broach, Klassic ONE 2237.01.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.02.010
FDA UDI
Class IIActive
Patella Calipers 2300.00.000
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 3, 10mm 5501.03.010
FDA UDI
Class IIActive
Klassic HD Acetabular Cup with Ti-Coat 3400.44.000
FDA UDI
Class IIActive
Klassic Knee Femur, Revision 6100.05.000
FDA UDI
Class IIActive
Klassic Femur, Nonporous 5105.03.000
FDA UDI
Class IIActive
Femoral Trial 2108.05.000
FDA UDI
Class IActive
Klassic Blade Neck Trial, Standard 1110.03.000
FDA UDI
Class IActive
Acetabular Shell with Ti-Coat, 64mm 3400.64.000
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert Trial 1228.64.036
FDA UDI
Class IActive
PS-Post Box Trial 2146.06.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.56.036
FDA UDI
Class IIActive
PS-Post Box Resection Guide 2172.04.000
FDA UDI
Class IActive
Klassic Domed Patella with E-Link 5502.01.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.010
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 3, 18 mm, Final Packed, Sterile 5300.03.018
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.03.005
FDA UDI
Class IIActive
Tibial Sizer 2202.03.000
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2170.05.000
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6403.02.005
FDA UDI
Class IIActive
Tibial Insert Trial 2205.02.010
FDA UDI
Class IActive
Klassic Blade Box Chisel 1336.00.000
FDA UDI
Class IActive
Femoral Cut Block 2106.04.000
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6403.07.005
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.56.036
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.