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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 9 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Femoral Augment, Posterior 6401.07.005
FDA UDI
Class IIActive
Femoral Head Impactor 1305.00.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.03.013
FDA UDI
Class IActive
Tibial Impactor Head 2115.00.200
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.021
FDA UDI
Class IActive
Klassic Tibial Augment & Screw 6405.05.005
FDA UDI
Class IIActive
Klassic Knee Tibial Baseplate Assembly, Size 3 5200.03.000
FDA UDI
Class IIActive
Tibial Insert Trial 2205.05.016
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 2 , 16mm 5204.02.016
FDA UDI
Class IIActive
Klassic HD Neck Trial, Offset 1105.03.000
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 6 3101.06.000
FDA UDI
Class IIActive
Spline Wrench 2017.00.000
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.56.036
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.36.350
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.03.024
FDA UDI
Class IActive
Klassic BiPolar Head, 50 mm OD, 28 mm Head 3205.50.028
FDA UDI
Class IIActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.03.000
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 1, 10mm 5501.01.010
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.60.036
FDA UDI
Class IIActive
Klassic Sombrero Patella with E-Link 5503.03.007
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2170.03.000
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.02.000
FDA UDI
Class IActive
Stem Trial 2015.18.170
FDA UDI
Class IActive
Stem Trial 2015.12.150
FDA UDI
Class IActive
Low Profile Tibial Cut Block, Right, Klassic ONE 2239.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.021
FDA UDI
Class IActive
All-Poly Tibial Broach, Klassic ONE 2245.01.000
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 1 3101.01.000
FDA UDI
Class IIActive
Femoral Trial 2108.07.000
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.06.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.03.012
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.04.010
FDA UDI
Class IActive
Distal Hip Reamer, Sz 16 1349.16.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.02.018
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.44.022
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.06.010
FDA UDI
Class IIActive
Sombrero Patella Trial 2307.04.007
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.06.016
FDA UDI
Class IIActive
Femoral Assembly Cradle 2804.00.000
FDA UDI
Class IActive
Klassic Tibial Baseplate with Ti-Coat, size 5 5202.05.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 3, 10 mm, Final Packed, Sterile 5300.03.010
FDA UDI
Class IIActive
Revision Tibial Baseplate Sizer and Trial 2903.06.000
FDA UDI
Class IActive
Modular AP Sizer Foot, 4 degree Right SRI-10036.R4
FDA UDI
Class IActive
Platform Neutral Acetabular Insert Trial 1226.58.036
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision 2126.02.000
FDA UDI
Class IActive
Klassic Blade Neck Trial, Standard 1110.01.000
FDA UDI
Class IActive
Klassic HD Neck Trial, Offset 1105.04.000
FDA UDI
Class IActive
Modular Broach Holder, Single Offset 1112.00.000
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6401.06.010
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2165.05.000
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.