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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 35 of 42
DeviceModel / ReferenceRegistriesClassStatus
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.021
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.46.028
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.46.028
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 1, 18 mm, Final Packed, Sterile 5300.01.018
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 1, 16 mm, Final Packed, Sterile 5300.01.016
FDA UDI
Class IIActive
Klassic Tibial Baseplate, Revision 6201.05.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.024
FDA UDI
Class IIActive
Femoral Cut Block, Pegless 2148.03.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.010
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.41.022
FDA UDI
Class IActive
Tibial Baseplate Trial 2204.04.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.016
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.013
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem, Porous, Size 4 3107.04.000
FDA UDI
Class IIActive
Cancellous Bone Screw with 6.5mm Head Diameter, 25mm 3600.25.065
FDA UDI
Class IIActive
Tibial Broach Stem, Starter 2203.00.013
FDA UDI
Class IActive
Klassic HD Acetabular Insert Trial 1204.46.022
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.36.000
FDA UDI
Class IActive
Knee Slaphammer 2006.00.000
FDA UDI
Class IActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.01.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.014
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert Trial 1228.60.036
FDA UDI
Class IActive
Augment Trial, Tibial 2902.05.005
FDA UDI
Class IActive
Klassic BiPolar Sizing Plate 1320.00.000
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.16.100
FDA UDI
Class IIActive
Distal Femoral Cut Guide, Fixed 2140.00.005
FDA UDI
Class IActive
Klassic Tibial Baseplate, Revision 6200.06.000
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.06.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.05.010
FDA UDI
Class IActive
Klassic Knee Tibial Stem Extension, 75mm 5600.00.075
FDA UDI
Class IIActive
Klassic Blade Femoral Broach 1109.07.000
FDA UDI
Class IActive
Klassic Tibial Baseplate, Revision 6201.04.000
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2165.03.000
FDA UDI
Class IActive
Klassic BiPolar Head, 55 mm OD, 28 mm Head 3205.55.028
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.02.014
FDA UDI
Class IActive
Tibial Sizer and Trial, Klassic ONE 2234.03.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with E-Link Poly 3502.44.022
FDA UDI
Class IIActive
Modular Tibial Broach, Klassic ONE 2237.03.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert Trial 1204.50.036
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.16.070
FDA UDI
Class IIActive
Klassic BiPolar Head, 56 mm OD, 28 mm Head 3205.56.028
FDA UDI
Class IIActive
28mm BIOLOX delta Ceramic Femoral Head, 12/14 taper 3203.28.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.013
FDA UDI
Class IActive
Tibial Alignment Guide, Upper Tower, Klassic ONE 2248.00.000
FDA UDI
Class IActive
Platform Acetabular Cup Sizer 1225.58.000
FDA UDI
Class IActive
36mm BIOLOX delta Femoral Head, 12/14 taper, +0mm Head Length 3203.36.000
FDA UDI
Class IIActive
Modular AP Sizer SRI-10035
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.05.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.012
FDA UDI
Class IActive
Stem Trial 2015.19.040
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.