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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 22 of 42
DeviceModel / ReferenceRegistriesClassStatus
Platform Hooded Acetabular Insert with E-Link 3512.52.036
FDA UDI
Class IIActive
Klassic Femur with Aurum 5104.01.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.012
FDA UDI
Class IIActive
Klassic HD Hip Offset Femoral Stem Trial 1316.09.000
FDA UDI
Class IActive
Platform Neutral Acetabular Insert with E-Link 3511.60.036
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.02.014
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.020
FDA UDI
Class IActive
Acetabular Cup Sizer 1200.52.000
FDA UDI
Class IActive
Stem Trial 2015.10.040
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.011
FDA UDI
Class IIActive
Cancellous Bone Screw with 6.5mm Head Diameter, 60mm 3600.60.065
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.018
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.012
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.05.018
FDA UDI
Class IActive
Notched Femur Impactor 2124.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.012
FDA UDI
Class IIActive
Acetabular Cup Sizer 1200.64.000
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 58mm 3501.58.032
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.012
FDA UDI
Class IActive
Flexion/Extension Cut Block, Klassic ONE 2159.00.000
FDA UDI
Class IActive
Klassic Knee Templates, Stem Extensions 2806.00.000
FDA UDI
Class IActive
Posterior Femoral Augment Trial 2809.05.010
FDA UDI
Class IActive
Stem Trial 2015.11.200
FDA UDI
Class IActive
Tibial Broach Stem 2203.00.100
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 6 , 12mm 5203.06.012
FDA UDI
Class IIActive
Acetabular Shell with Ti-Coat, 62mm 3400.62.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 1, 16 mm, Final Packed, Sterile 5301.01.016
FDA UDI
Class IIActive
Pin Puller 2005.00.000
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.32.035
FDA UDI
Class IActive
Revision Tibial Baseplate Sizer and Trial 2903.01.000
FDA UDI
Class IActive
PS-Post Box Trial, Klassic ONE 2171.07.000
FDA UDI
Class IActive
Cancellous Bone Screw with 6.5mm Head Diameter, 35mm 3600.35.065
FDA UDI
Class IIActive
Klassic Knee Domed Patella, Size 4 5500.04.000
FDA UDI
Class IIActive
Femoral Head Trial 1306.32.035
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.010
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.018
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.05.008
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2170.06.000
FDA UDI
Class IActive
Stem Trial 2015.10.070
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.018
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert with E-Link 3512.60.036
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.013
FDA UDI
Class IActive
Klassic BiPolar Head, 49 mm OD, 28 mm Head 3205.49.028
FDA UDI
Class IIActive
Klassic Femur with Aurum 5104.04.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.03.016
FDA UDI
Class IActive
Pin Diver, Triangle 2013.00.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 6 , 10mm 5204.06.010
FDA UDI
Class IIActive
Stem Trial 2015.20.070
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.55.000
FDA UDI
Class IActive
Stem Trial 2015.12.200
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.