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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
—
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 41 of 42
DeviceModel / ReferenceRegistriesClassStatus
Acetabular Cup Sizer 1200.46.000
FDA UDI
Class IActive
Tibial Baseplate Trial, Flat 2204.01.100
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.03.013
FDA UDI
Class IActive
Klassic ONE Universal Cone & Revision Baseplate Tray, Pin Mat Insert 2417.00.100
FDA UDI
Class IActive
Intramedullary Reamer 2014.11.000
FDA UDI
Class IActive
Klassic Tibial Augment 6404.01.005
FDA UDI
Class IIActive
Low Profile Tibial Cut Block, Left, Klassic ONE 2238.00.000
FDA UDI
Class IActive
Distal Hip Reamer, Sz 15 1349.15.000
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6400.04.010
FDA UDI
Class IIActive
Distal Hip Reamer, Sz 6 1349.06.000
FDA UDI
Class IActive
Klassic BiPolar Head Extractor 1324.00.000
FDA UDI
Class IActive
PS-Post Box Trial, Klassic ONE 2165.06.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.05.012
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 2, 7mm 5501.02.007
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 6, 10 mm, Final Packed, Sterile 5300.06.010
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.018
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.04.011
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.02.016
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6400.01.005
FDA UDI
Class IIActive
Bent Retractor 2001.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.04.024
FDA UDI
Class IIActive
Tibial Insert Trial 2205.02.014
FDA UDI
Class IActive
32mm Femoral Head, 12/14 Taper, +7mm Offset 3200.32.700
FDA UDI
Class IIActive
Posterior Femoral Augment Trial 2809.03.005
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.012
FDA UDI
Class IActive
Klassic HD Acetabular Insert Trial 1204.46.032
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.47.000
FDA UDI
Class IActive
Stem Trial 2015.16.120
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.54.036
FDA UDI
Class IIActive
Klassic Femur, Nonporous 5105.07.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 1, 10 mm, Final Packed, Sterile 5301.01.010
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.016
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.014
FDA UDI
Class IActive
Klassic Femur, Porous, Klassic Tibial Baseplate, Porous K162256
FDA 510(k)
Class IIActive
Klassic Knee System Tibial Inserts, PS-Max K202740
FDA 510(k)
Class IIActive
Klassic HD® Hip System K180929
FDA 510(k)
Class IIActive
Platform® Acetabular System K220483
FDA 510(k)
Class IIActive
Klassic Knee System K153310
FDA 510(k)
Class IIActive
Klassic HD Hip System K151440
FDA 510(k)
Class IIActive
Klassic Hd(tm) Extended Offset Femoral Head K131454
FDA 510(k)
Class IIActive
Klassic HD® Hip System K171962
FDA 510(k)
Class IIActive
Klassic Hd Hip System, Offset Femoral Stem, Non-Porous / Porous K133832
FDA 510(k)
Class IIActive
Klassic Knee System K211877
FDA 510(k)
Class IIActive
Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® Poly K173104
FDA 510(k)
Class IIActive
Klassic BiPolar System K143113
FDA 510(k)
Class IIActive
Klassic Knee System K162422
FDA 510(k)
Class IIActive
Klassic® Knee System K180159
FDA 510(k)
Class IIActive
Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post K232414
FDA 510(k)
Class IIActive
Adapter Sleeve for BIOLOX® OPTION Femoral Head, +10.5mm head length K213580
FDA 510(k)
Class IIActive
BIOLOX CONTOURA Ceramic Femoral Head K191399
FDA 510(k)
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.