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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
—
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 28 of 42
DeviceModel / ReferenceRegistriesClassStatus
Femoral Cut Block, Narrow 2139.03.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.013
FDA UDI
Class IActive
Klassic Knee Femur, Size 1, Nonporous 5100.01.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.013
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.02.013
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.014
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.05.016
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.62.032
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem, Porous, Size 3 3107.03.000
FDA UDI
Class IIActive
28mm Femoral Head, 12/14 taper, +7mm offset 3200.28.700
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.01.021
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.52.036
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.02.016
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 2 3103.02.000
FDA UDI
Class IIActive
Tibial Baseplate Trial 2204.02.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.01.024
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.022
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 2, 14 mm, Final Packed, Sterile 5301.02.014
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.57.028
FDA UDI
Class IActive
Klassic HD Modular Femoral Broach 1106.02.000
FDA UDI
Class IActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.36.000
FDA UDI
Class IIActive
Platform Acetabular Cup with Ti-Coat 3401.54.000
FDA UDI
Class IIActive
Acetabular Insert Trial 1204.52.036
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 2, 12 mm, Final Packed, Sterile 5300.02.012
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 58mm 3503.58.032
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.05.016
FDA UDI
Class IIActive
Modular Knee Impactor Head, All-Poly 2128.00.000
FDA UDI
Class IActive
Femoral Cut Block 2106.03.000
FDA UDI
Class IActive
Klassic Femur with Aurum 5104.02.000
FDA UDI
Class IIActive
Adapter for BIOLOX OPTION Femoral Head, +3.5mm head length 3301.00.350
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.03.016
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.018
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2164.04.000
FDA UDI
Class IActive
Stem Trial 2015.14.150
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.28.350
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.64.036
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.06.005
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.014
FDA UDI
Class IIActive
Tibial Stem Extension Reamer 2209.00.150
FDA UDI
Class IActive
BiPolar Femoral Head Trial 1326.22.350
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.45.028
FDA UDI
Class IActive
Klassic ONE Knee PS-Post Primary Instrumentation Tray 2411.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.016
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.44.022
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 58mm 3503.58.036
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 1 , 10mm 5203.01.010
FDA UDI
Class IIActive
Alignment Tower 2103.00.000
FDA UDI
Class IActive
Femoral Head Trial 1306.36.700
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 2 , 12mm 5204.02.012
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.01.010
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.