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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
—
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 29 of 42
DeviceModel / ReferenceRegistriesClassStatus
Tibial Reamer, Klassic ONE 2247.00.000
FDA UDI
Class IActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 7 3103.07.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.05.010
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 3, 14 mm, Final Packed, Sterile 5301.03.014
FDA UDI
Class IIActive
Klassic Knee Femur, Size 2, Nonporous 5100.02.000
FDA UDI
Class IIActive
Pin Driver, 2.5mm Hex 2007.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.018
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.12.050
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.18.100
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.56.036
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2165.04.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.012
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with E-Link Poly 3502.46.022
FDA UDI
Class IIActive
Stem Trial 2015.16.100
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.013
FDA UDI
Class IIActive
Tibial Insert Trial 2205.05.014
FDA UDI
Class IActive
Femoral Stem Adapter Reamer Guide 2802.00.000
FDA UDI
Class IActive
Modular Cone Reamer, Handle 2019.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.04.014
FDA UDI
Class IIActive
Klassic Augment Screw 6406.00.010
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.03.024
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.52.032
FDA UDI
Class IIActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 6 5201.06.000
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 1 , 16mm 5203.01.016
FDA UDI
Class IIActive
Klassic HD Modular Femoral Broach 1106.00.000
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6402.03.005
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.011
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 1 , 16mm 5204.01.016
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.013
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.64.036
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.014
FDA UDI
Class IActive
Klassic Knee Tibial Stem Extension, 25mm 5600.00.025
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D, size 6 5102.06.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 3, 14 mm, Final Packed, Sterile 5300.03.014
FDA UDI
Class IIActive
Klassic HD Neck Trial, Standard 1104.01.000
FDA UDI
Class IActive
Klassic Tibial Augment 6404.03.005
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.02.011
FDA UDI
Class IActive
Klassic Knee Domed Patella, Size 3 5500.03.000
FDA UDI
Class IIActive
Modular Liner Impactor Head 1222.28.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 6, 16 mm, Final Packed, Sterile 5301.06.016
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.020
FDA UDI
Class IIActive
Klassic BiPolar Trial 1322.50.028
FDA UDI
Class IActive
Modular Reamer Driver, Klassic ONE 2167.00.000
FDA UDI
Class IActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 56mm 3502.56.032
FDA UDI
Class IIActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.06.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 1, 14 mm, Final Packed, Sterile 5300.01.014
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.014
FDA UDI
Class IActive
Universal Cone Trial, Size 7, 24° 2022.07.024
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.013
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 5, 16 mm, Final Packed, Sterile 5300.05.016
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.