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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 7 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Tibial Insert, Ultra-PS, Size 2, 10 mm, Final Packed, Sterile 5301.02.010
FDA UDI
Class IIActive
Femoral Cut Block, Pegless 2148.07.000
FDA UDI
Class IActive
Cancellous Bone Screw with 6.5mm Head Diameter, 55mm 3600.55.065
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.021
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.06.016
FDA UDI
Class IActive
Tibial Stem Extension Reamer 2209.00.075
FDA UDI
Class IActive
Klassic HD Hip Offset Femoral Stem Trial 1316.05.000
FDA UDI
Class IActive
Distal Hip Reamer, Sz 13 1349.13.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.016
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 64mm 3501.64.036
FDA UDI
Class IIActive
Tibial Alignment Guide - Spiked Upper Tower, Klassic ONE 2244.00.000
FDA UDI
Class IActive
Femoral Cut Block, Narrow 2139.02.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.012
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.03.012
FDA UDI
Class IActive
Modular Femoral Head Trial 1326.36.000
FDA UDI
Class IActive
PS-Post Box Resection Guide 2172.06.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.022
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.010
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.46.022
FDA UDI
Class IIActive
Klassic Augment Screw 6406.00.005
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.010
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 5, 14 mm, Final Packed, Sterile 5301.05.014
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.16.050
FDA UDI
Class IIActive
Klassic Femoral Augment Screw, Distal 6407.00.010
FDA UDI
Class IIActive
Tibial Sizer 2202.02.000
FDA UDI
Class IActive
Fluted Pin, Square Head, 89mm 2707.00.089
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.44.028
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.44.028
FDA UDI
Class IActive
Stem Trial 2015.13.200
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.01.000
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.02.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.021
FDA UDI
Class IActive
Klassic Tibial Augment & Screw 6405.03.005
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D 5106.03.000
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.32.035
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.013
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.018
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.021
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.02.012
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.020
FDA UDI
Class IIActive
PS-Post Box Trial 2146.04.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.012
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.50.032
FDA UDI
Class IIActive
Distal Femoral Cut Guide, Fixed 2140.00.006
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegless 2204.02.200
FDA UDI
Class IActive
Klassic Knee Tibial Baseplate Assembly, Size 4 5200.04.000
FDA UDI
Class IIActive
Universal Cone Impactor Head, Size 4, 18° 2021.04.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.01.022
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.016
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.