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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 38 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic BiPolar Head, 60 mm OD, 28 mm Head 3205.60.028
FDA UDI
Class IIActive
Klassic Femur with Aurum 5104.07.000
FDA UDI
Class IIActive
6 Degree Locking Upper Tibial Alignment Guide, Klassic ONE SRI-10033
FDA UDI
Class IActive
PS-Post Box Resection Guide 2145.02.000
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.32.350
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.010
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.54.036
FDA UDI
Class IIActive
Klassic Knee Femur, Size 3, Nonporous 5100.03.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 41 mm OD, 22 mm Head 3205.41.022
FDA UDI
Class IIActive
36mm Femoral Head, 12/14 Taper, +3.5mm Offset 3200.36.350
FDA UDI
Class IIActive
Adapter for BIOLOX OPTION Femoral Head, +0mm head length 3301.00.000
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.36.105
FDA UDI
Class IActive
Modular Slap Hammer Extractor Impactor, Klassic ONE 2011.00.000
FDA UDI
Class IActive
Klassic Knee Case 3, Patella/Misc. Preparation Instrumentation 2403.00.000
FDA UDI
Class IActive
Klassic Blade Femoral Stem Impactor, Angled Tip 1334.00.000
FDA UDI
Class IActive
Klassic Femur with Cobalt 3D 5106.07.000
FDA UDI
Class IIActive
Posterior Femoral Augment Trial 2809.01.010
FDA UDI
Class IActive
Tibial Sizer and Trial, Klassic ONE 2234.04.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.62.032
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.014
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 6, 14 mm, Final Packed, Sterile 5301.06.014
FDA UDI
Class IIActive
Acetabular Insert Trial 1204.48.032
FDA UDI
Class IActive
All-Poly Tibial Broach, Klassic ONE 2245.05.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE 3503.46.028
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.04.018
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 3 , 16mm 5204.03.016
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.02.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.024
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.014
FDA UDI
Class IActive
Universal Cone Impactor Head 2021.34.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.01.016
FDA UDI
Class IActive
Distal Femoral Cut Guide, Fixed with Paddles 2140.00.105
FDA UDI
Class IActive
PS-Post Box Trial, Klassic ONE 2165.07.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.05.013
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.36.350
FDA UDI
Class IActive
3.5mm Hex Screwdriver, Klassic ONE 2241.00.000
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.43.000
FDA UDI
Class IActive
Stem Trial 2015.16.150
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.011
FDA UDI
Class IActive
Klassic HD Offset Femur Provisional Case 1408.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.18.070
FDA UDI
Class IIActive
Hooded Acetabular Insert Trial 1223.50.036
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.14.040
FDA UDI
Class IIActive
Femoral Stem Extractor Hoop 1303.00.000
FDA UDI
Class IActive
Intramedullary Reamer 2014.14.000
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.03.010
FDA UDI
Class IIActive
Tibial Insert Trial 2205.01.012
FDA UDI
Class IActive
Platform Hooded Acetabular Insert with E-Link 3512.50.032
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.50.036
FDA UDI
Class IActive
Acetabular Angled Drill Guide 1220.00.000
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.