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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 16 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.02.014
FDA UDI
Class IIActive
Modular Impactor Handle 2125.00.000
FDA UDI
Class IActive
Klassic Knee Tibial Stem Extension, 100mm 5600.00.100
FDA UDI
Class IIActive
Tibial Sizer and Trial, Klassic ONE 2234.06.000
FDA UDI
Class IActive
Distal Hip Reamer, Sz 7 1349.07.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.56.032
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 1 3103.01.000
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 6 , 10mm 5203.06.010
FDA UDI
Class IIActive
Femoral Stem Adapter Reamer 2801.00.000
FDA UDI
Class IActive
Klassic Knee Tibial Stem Extension, 150mm 5600.00.150
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.64.036
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.63.000
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.54.032
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.05.016
FDA UDI
Class IActive
Distal Hip Reamer, Sz 20 1349.20.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.024
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.021
FDA UDI
Class IIActive
Klassic BiPolar Sizing Handle 1323.22.000
FDA UDI
Class IActive
PS-Post Box Trial 2146.02.000
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.54.036
FDA UDI
Class IActive
Klassic Stem Adapter, Femoral 6602.00.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.03.018
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.03.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 2 , 16mm 5203.02.016
FDA UDI
Class IIActive
Platform Acetabular Cup with Ti-Coat 3401.50.000
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.60.036
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.07.010
FDA UDI
Class IIActive
28mm Femoral Head, 12/14 taper, -3.5mm offset 3200.28.035
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.013
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.44.028
FDA UDI
Class IIActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 2 5201.02.000
FDA UDI
Class IIActive
Klassic Femur, PS-Post 5101.06.000
FDA UDI
Class IIActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 5 3101.05.000
FDA UDI
Class IIActive
Femoral Head Trial 1306.36.350
FDA UDI
Class IActive
Stem Trial 2015.18.040
FDA UDI
Class IActive
28mm BIOLOX OPTION Ceramic Revision Femoral Head, 16/18 taper 3204.28.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.04.010
FDA UDI
Class IIActive
Femoral Broach 1100.07.000
FDA UDI
Class IActive
Klassic Knee Sombrero Patella 5501.05.010
FDA UDI
Class IIActive
Femoral Head Trial 1306.32.700
FDA UDI
Class IActive
Klassic HD Modular Femoral Broach 1106.04.000
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 50mm 3501.50.032
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 54mm 3503.54.036
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 5, 14 mm, Final Packed, Sterile 5300.05.014
FDA UDI
Class IIActive
Platform Acetabular Cup with Ti-Coat 3401.58.000
FDA UDI
Class IIActive
Klassic ONE Universal Cone & Revision Baseplate Instrumentation Tray 2417.00.000
FDA UDI
Class IActive
MIS Cut Block Modified, Left SRI-10038
FDA UDI
Class IActive
28mm Femoral Head, 12/14 taper, +0mm offset 3200.28.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 52 mm OD, 28 mm Head 3205.52.028
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2171.01.000
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.