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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 27 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic HD Acetabular Insert with E-Link Poly 3502.44.028
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.020
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.024
FDA UDI
Class IActive
Klassic Blade Femoral Stem, Porous, Size 3 3105.03.000
FDA UDI
Class IIActive
Stem Trial 2015.17.120
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 4 , 14mm 5204.04.014
FDA UDI
Class IIActive
Universal Cone 6800.05.024
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.014
FDA UDI
Class IActive
Tibial Insert Trial 2205.03.011
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 54mm 3501.54.036
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.06.010
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with E-Link Poly 3502.46.028
FDA UDI
Class IIActive
Klassic BiPolar Head, 57 mm OD, 28 mm Head 3205.57.028
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert with E-Link 3512.46.032
FDA UDI
Class IIActive
Acetabular Shell with Ti-Coat, 50mm 3400.50.000
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE 3503.46.022
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.54.032
FDA UDI
Class IIActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.03.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.020
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.03.012
FDA UDI
Class IIActive
Distal Hip Reamer, Sz 9 1349.09.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.54.036
FDA UDI
Class IIActive
Curved Acetabular Cup Impactor 1213.00.000
FDA UDI
Class IActive
Klassic BiPolar Head, 39 mm OD, 22 mm Head 3205.39.022
FDA UDI
Class IIActive
Stem Impaction Adapter 1344.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.20.100
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.013
FDA UDI
Class IActive
Platform Acetabular Cup with Ti-Coat 3401.60.000
FDA UDI
Class IIActive
Tibial Insert Trial 2205.06.013
FDA UDI
Class IActive
Tibial Baseplate Trial, Flat 2204.02.100
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.48.032
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.54.036
FDA UDI
Class IIActive
Universal Cone Trial, Size 6, 24° 2022.06.024
FDA UDI
Class IActive
3-in-1 Drill 2113.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.06.014
FDA UDI
Class IIActive
Acetabular Angled Drill Driver 1218.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.03.011
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.012
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 3, 18 mm, Final Packed, Sterile 5301.03.018
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.012
FDA UDI
Class IIActive
Klassic HD Neck Trial, Standard 1104.04.000
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.05.018
FDA UDI
Class IActive
32mm BIOLOX delta Femoral Head, 12/14 taper, +0mm Head Length 3203.32.000
FDA UDI
Class IIActive
Tibial Sizer and Trial, Klassic ONE 2234.01.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.013
FDA UDI
Class IIActive
Contoura Femoral Head Trial 1347.28.035
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 4 , 12mm 5203.04.012
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem, Porous, Size 5 3107.05.000
FDA UDI
Class IIActive
Cancellous Bone Screw with 6.5mm Head Diameter, 30mm 3600.30.065
FDA UDI
Class IIActive
Klassic BiPolar Head, 38 mm OD, 22 mm Head 3205.38.022
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.