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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 19 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Femoral Augment, Posterior 6401.02.005
FDA UDI
Class IIActive
Klassic HD Hip Case 3, Acetabular Reamer and Miscellaneous Instruments, AL 1407.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.01.012
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.56.036
FDA UDI
Class IIActive
Distal Femoral Cut Guide SSI-10028
FDA UDI
Class IActive
PS-Post Box Resection Guide 2145.04.000
FDA UDI
Class IActive
All-Poly Tibial Broach Tower Assembly 2215.05.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 4, 16 mm, Final Packed, Sterile 5301.04.016
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.010
FDA UDI
Class IActive
Klassic Femur with Aurum 5104.03.000
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.62.036
FDA UDI
Class IIActive
Stem Trial 2015.13.050
FDA UDI
Class IActive
Stem Trial 2015.19.200
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.024
FDA UDI
Class IIActive
Klassic Knee Domed Patella, Size 1 5500.01.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.02.021
FDA UDI
Class IActive
PS-Post Box Trial, Klassic ONE 2171.04.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.50.028
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.52.028
FDA UDI
Class IActive
Stem Trial 2015.11.050
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.014
FDA UDI
Class IIActive
Klassic BiPolar Head, 59 mm OD, 28 mm Head 3205.59.028
FDA UDI
Class IIActive
Femoral Trial, PS-Post/Revision, Klassic ONE 2170.02.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.014
FDA UDI
Class IActive
Drill 2003.00.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 56mm 3503.56.036
FDA UDI
Class IIActive
Varus/Valgus Cut Block 2212.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.02.016
FDA UDI
Class IIActive
Tibial Insert Trial 2205.03.010
FDA UDI
Class IActive
Stem Trial 2015.13.120
FDA UDI
Class IActive
Tibial Stylus 2207.00.000
FDA UDI
Class IActive
Klassic Knee PS-Max, Stems/Augments Instrumentation Tray 2414.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.016
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 64mm 3503.64.032
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.021
FDA UDI
Class IActive
Klassic Tibial Insert Set Screw, for Primary or Revision 5603.00.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 1, 18 mm, Final Packed, Sterile 5301.01.018
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 60mm 3502.60.032
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.01.013
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.46.032
FDA UDI
Class IActive
PS-Post Box Reamer, Trephine 2142.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.016
FDA UDI
Class IActive
Platform Acetabular Cup Sizer 1225.50.000
FDA UDI
Class IActive
Klassic Blade Box Chisel, Curved 1338.00.000
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.05.012
FDA UDI
Class IActive
Revision Tibial Baseplate Sizer and Trial 2903.05.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.010
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.44.022
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.06.010
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.