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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 23 of 42
DeviceModel / ReferenceRegistriesClassStatus
Modular Femoral Head Trial 1326.32.035
FDA UDI
Class IActive
8mm Drill 2111.00.000
FDA UDI
Class IActive
Stem Trial 2015.10.050
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.02.024
FDA UDI
Class IActive
Femoral Head Trial 1306.36.035
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 50mm 3503.50.032
FDA UDI
Class IIActive
Femoral Head Remover, Corkscrew 1339.00.000
FDA UDI
Class IActive
Stem Trial 2015.11.040
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.12.070
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.60.032
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.03.013
FDA UDI
Class IActive
Klassic Femur with Cobalt 3D 5106.02.000
FDA UDI
Class IIActive
Hemispherical Acetabular Reamer 1207.58.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.46.028
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.013
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.05.010
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 62mm 3501.62.036
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem, Porous, Size 6 3107.06.000
FDA UDI
Class IIActive
Tibial Resection Tower 2907.00.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.49.028
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.010
FDA UDI
Class IIActive
Tibial Baseplate Trial, Pegless 2204.03.200
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 4, 10 mm, Final Packed, Sterile 5301.04.010
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 3 , 10mm 5203.03.010
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.44.028
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.44.028
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.54.032
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 50mm 3502.50.032
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 3, 12 mm, Final Packed, Sterile 5301.03.012
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 4 , 14mm 5203.04.014
FDA UDI
Class IIActive
Modular AP Sizer Foot, 4 degree Left SRI-10036.L4
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 3, 10 mm, Final Packed, Sterile 5301.03.010
FDA UDI
Class IIActive
Screw Pin, Hex Head, 33mm 2706.00.033
FDA UDI
Class IActive
Femoral Cut Block, Pegless 2148.02.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.016
FDA UDI
Class IActive
Modular Distal Femoral Cut Guide Fixed 2149.00.004
FDA UDI
Class IActive
Tibial Alignment Guide - Upper Tower 2201.00.000
FDA UDI
Class IActive
Sombrero Patella Trial 2307.01.007
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.12.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.03.011
FDA UDI
Class IActive
Universal Cone Impactor Head, Size 7, 24° 2021.07.024
FDA UDI
Class IActive
Tibial Broach 2203.01.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.04.018
FDA UDI
Class IIActive
Sombrero Patella Trial 2307.02.010
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.38.022
FDA UDI
Class IActive
Tibial Sizer 2202.01.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert Trial 1204.46.028
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.08.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.012
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.12.150
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.