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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 33 of 42
DeviceModel / ReferenceRegistriesClassStatus
Intramedullary Reamer, Revision 2026.14.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.016
FDA UDI
Class IActive
PS-Post Box Resection Guide 2145.06.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.39.022
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.36.035
FDA UDI
Class IActive
Tibial Insert Trial 2205.02.012
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.013
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.04.012
FDA UDI
Class IActive
Tibial Insert Trial 2205.02.018
FDA UDI
Class IActive
Acetabular Reamer Driver, Offset 1209.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.021
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.022
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.011
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.016
FDA UDI
Class IActive
Quick Pin, Sharp 2004.30.200
FDA UDI
Class IActive
Distal Hip Reamer, Sz 14 1349.14.000
FDA UDI
Class IActive
Tibial Alignment Guide - 3 degrees Spike Upper Tower, Klassic ONE 2257.00.000
FDA UDI
Class IActive
3.2mm Drill with Stop 2009.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.013
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.011
FDA UDI
Class IActive
Varus/Valgus Cut Block, Klassic ONE 2243.00.000
FDA UDI
Class IActive
Acetabular Based Retractor SRI-10034
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.010
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.20.200
FDA UDI
Class IIActive
Klassic Knee Sombrero Patella, Size 3, 7mm 5501.03.007
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.58.032
FDA UDI
Class IIActive
Tibial Insert Trial 2205.04.011
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.014
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.48.032
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.024
FDA UDI
Class IIActive
Klassic Knee Case 2, Tibial Preparation Instrumentation 2406.00.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.58.036
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 3, 16 mm, Final Packed, Sterile 5300.03.016
FDA UDI
Class IIActive
Universa Cone Impactor Head, Size 2, 12° 2021.02.012
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.04.012
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.04.005
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.58.036
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 5 , 10mm 5203.05.010
FDA UDI
Class IIActive
Tibial Insert Trial 2205.01.018
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.01.013
FDA UDI
Class IActive
Klassic Knee Case 1, Femoral Preparation Instrumentation 2405.00.000
FDA UDI
Class IActive
OrthoGroup Double Offset Broach Holder, Right 1117.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.05.012
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.02.018
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.56.032
FDA UDI
Class IIActive
Klassic Sombrero Patella with E-Link 5503.02.010
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 36mm Head, Size 64mm 3502.64.036
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.012
FDA UDI
Class IIActive
Femoral Broach 1100.03.000
FDA UDI
Class IActive
Femoral Cut Block, Narrow 2139.04.000
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.