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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 40 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Stem Extension, Cemented 6600.20.070
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.013
FDA UDI
Class IIActive
Modular Distal Femoral Cut Guide Fixed 2149.00.005
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6403.01.010
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE 3503.44.028
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.06.011
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.06.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.05.024
FDA UDI
Class IActive
Stem Trial 2015.18.120
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.01.016
FDA UDI
Class IActive
Intramedullary Reamer, Revision 2026.17.000
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 2 3101.02.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.03.005
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.18.000
FDA UDI
Class IActive
Contoura Femoral Head Trial 1347.36.700
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.14.100
FDA UDI
Class IIActive
Acetabular Cup Positioner, Handle 1203.00.000
FDA UDI
Class IActive
Tibial Baseplate Trial 2204.05.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.64.032
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.014
FDA UDI
Class IIActive
Femoral Augment Alignment Guide 2016.00.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.46.022
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.06.010
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6400.05.005
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.38.022
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.16.120
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.46.028
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.50.032
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.62.032
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 6, 18 mm, Final Packed, Sterile 5301.06.018
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.64.032
FDA UDI
Class IIActive
Femoral Broach 1100.05.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 5 , 12mm 5203.05.012
FDA UDI
Class IIActive
Femoral X-Ray Templates 1312.00.000
FDA UDI
Class IActive
32mm Femoral Head, 12/14 Taper, +3.5mm Offset 3200.32.350
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.03.014
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.58.036
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.44.028
FDA UDI
Class IActive
Klassic HD Hip Offset Femoral Stem Trial 1316.06.000
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.06.000
FDA UDI
Class IActive
Modular Knee Impactor Head, Universal 2129.00.000
FDA UDI
Class IActive
Klassic Femur with Cobalt 3D, size 2 5102.02.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.02.011
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D, size 1 5102.01.000
FDA UDI
Class IIActive
Posterior Femoral Augment Trial 2809.05.005
FDA UDI
Class IActive
Klassic HD Modular Femoral Broach 1106.03.000
FDA UDI
Class IActive
Klassic Tibial Baseplate with Ti-Coat, size 1 5202.01.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 51 mm OD, 28 mm Head 3205.51.028
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.021
FDA UDI
Class IActive
Klassic Knee Tibial Baseplate Assembly, Size 6 5200.06.000
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.