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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 6 of 42
DeviceModel / ReferenceRegistriesClassStatus
Femoral Stem Impactor with Anteversion 1307.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.16.150
FDA UDI
Class IIActive
Universal Cone X-Ray Template 2025.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.18.150
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.016
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.010
FDA UDI
Class IIActive
Sombrero Patella Trial 2307.03.007
FDA UDI
Class IActive
Femoral Broach 1100.06.000
FDA UDI
Class IActive
Klassic Femur, Nonporous 5105.04.000
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.10.120
FDA UDI
Class IIActive
Femoral Broach 1100.02.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.013
FDA UDI
Class IIActive
Klassic BiPolar Head, 44 mm OD, 28 mm Head 3205.44.028
FDA UDI
Class IIActive
Modular Hip Impactor Head, Femoral Head 1342.00.000
FDA UDI
Class IActive
Stem Trial 2015.19.050
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.04.012
FDA UDI
Class IIActive
Angel Wing 2112.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.014
FDA UDI
Class IIActive
Thread Adaptor 1318.00.000
FDA UDI
Class IActive
Klassic Blade Neck Trial, Standard 1110.02.000
FDA UDI
Class IActive
Klassic Knee Femur, Size 5, Nonporous 5100.05.000
FDA UDI
Class IIActive
Tibial Alignment Guide, 3 Degree Upper Tower 2258.00.000
FDA UDI
Class IActive
Modular Slap Hammer Rod, Klassic ONE 2010.00.000
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.48.036
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 6, 16 mm, Final Packed, Sterile 5300.06.016
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.06.016
FDA UDI
Class IIActive
Acetabular Shell with Ti-Coat, 54mm 3400.54.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.06.014
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.011
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.05.016
FDA UDI
Class IActive
Femoral Cut Block, Pegless 2148.05.000
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.48.032
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 5 , 12mm 5204.05.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.04.024
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.52.032
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert with E-Link 3512.58.036
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.60.032
FDA UDI
Class IIActive
Klassic Tibial Baseplate with Ti-Coat, size 4 5202.04.000
FDA UDI
Class IIActive
Intramedullary Reamer 2014.10.000
FDA UDI
Class IActive
Stem Trial 2015.17.170
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.024
FDA UDI
Class IActive
22mm Femoral Head, 12/14 taper, +7mm offset 3200.22.700
FDA UDI
Class IIActive
Intramedullary Resection Guide Adapter 2906.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.014
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.02.012
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.02.016
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.32.700
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.01.024
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.46.022
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 60mm 3501.60.036
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.