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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
—
LinkedIn
—
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 26 of 42
DeviceModel / ReferenceRegistriesClassStatus
Stem Trial 2015.11.120
FDA UDI
Class IActive
Platform Neutral Acetabular Insert Trial 1226.48.032
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.06.011
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 4, 14 mm, Final Packed, Sterile 5301.04.014
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.06.014
FDA UDI
Class IActive
Stem Trial 2015.15.100
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.55.028
FDA UDI
Class IActive
Modular Liner Impactor Head 1222.32.000
FDA UDI
Class IActive
Femur Trial 2147.06.000
FDA UDI
Class IActive
Femoral Broach 1100.04.000
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.32.350
FDA UDI
Class IActive
Cancellous Bone Screw with 6.5mm Head Diameter, 15mm 3600.15.065
FDA UDI
Class IIActive
PS-Post Box Trial 2146.07.000
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.36.700
FDA UDI
Class IIActive
Klassic HD Hip Case 1, Femur Instruments 1405.00.000
FDA UDI
Class IActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 52mm 3502.52.032
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.01.000
FDA UDI
Class IActive
Klassic HD Neck Trial, Standard 1104.02.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.10.150
FDA UDI
Class IIActive
PS-Post Box Reamer, Trephine, Klassic ONE 2166.00.000
FDA UDI
Class IActive
Domed Femur/Tibia Impactor Head 2115.00.100
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 6 , 12mm 5204.06.012
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.02.014
FDA UDI
Class IIActive
Klassic Blade Femoral Stem, Porous, Size 7 3105.07.000
FDA UDI
Class IIActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 3 5201.03.000
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 62mm 3502.62.032
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.014
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.01.012
FDA UDI
Class IActive
Acetabular Insert Trial 1204.60.036
FDA UDI
Class IActive
Distal Hip Reamer, Sz 8 1349.08.000
FDA UDI
Class IActive
Acetabular Shell with Ti-Coat, 60mm 3400.60.000
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.05.013
FDA UDI
Class IActive
Klassic HD Acetabular Insert Trial 1204.44.028
FDA UDI
Class IActive
BiPolar Femoral Head Trial 1326.28.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.45.028
FDA UDI
Class IActive
Spline Wrench, Closed 2017.00.100
FDA UDI
Class IActive
Tibial Stem Extension Reamer 2211.00.000
FDA UDI
Class IActive
Modular Femoral Head Trial 1326.32.350
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.50.000
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.32.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.02.011
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.014
FDA UDI
Class IIActive
Klassic BiPolar Head, 40 mm OD, 22 mm Head 3205.40.022
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.010
FDA UDI
Class IIActive
Acetabular Shell with Ti-Coat, 58mm 3400.58.000
FDA UDI
Class IIActive
Modular Femoral Head Trial 1326.36.350
FDA UDI
Class IActive
Alignment Rod 2104.00.000
FDA UDI
Class IActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 4 5201.04.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.016
FDA UDI
Class IActive
Platform Neutral Acetabular Insert Trial 1226.50.032
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.