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TOTAL JOINT ORTHOPEDICS, INC.

Last updated September 17, 2026

Information

Country: US
Address: 1567 E. Stratford Avenue, Salt Lake City, UT, 84106
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EUDAMED SRN: —
FDA FEI Number: 3008544874
DUNS Number: —

Catalogue (2063)

Page 18 of 42

Device	Model / Reference	Registries	Class	Status
Klassic Tibial Insert, Ultra-PS, E-Link Poly	5303.03.014	FDA UDI	Class II	Active
Klassic Tibial Insert, PS-Post, E-Link	5305.03.016	FDA UDI	Class II	Active
Tibial Insert Trial, PS-Max, Klassic ONE	2252.01.013	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Max, Std Poly	6300.01.022	FDA UDI	Class II	Active
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 4 , 16mm	5203.04.016	FDA UDI	Class II	Active
Intramedullary Reamer	2014.20.000	FDA UDI	Class I	Active
Klassic Knee Primary Tray	2408.00.000	FDA UDI	Class I	Active
Platform Neutral Acetabular Insert Trial	1226.60.036	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Post, E-Link Poly	5305.04.024	FDA UDI	Class II	Active
Klassic HD Low Profile Acetabular Insert with XLPE Poly	3510.54.032	FDA UDI	Class II	Active
Notched Femur Impactor, PS-Post	2151.00.000	FDA UDI	Class I	Active
Klassic Stem Extension, Cemented	6600.14.050	FDA UDI	Class II	Active
Klassic Tibial Insert, PS-Post, Std Poly	5304.06.024	FDA UDI	Class II	Active
Revision Modular Tibial Broach	2905.01.000	FDA UDI	Class I	Active
Femur/Tibia Implant Impactor Head	2115.00.000	FDA UDI	Class I	Active
Klassic Tibial Insert, Ultra-PS, E-Link Poly	5303.02.013	FDA UDI	Class II	Active
Offset Femoral Stem X-Ray Templates	1319.00.000	FDA UDI	Class I	Active
Klassic HD Hooded Acetabular Insert with XLPE Poly	3508.64.032	FDA UDI	Class II	Active
Klassic BiPolar Trial	1322.53.028	FDA UDI	Class I	Active
Klassic Knee Tibial Insert, Ultra-PS, Size 4, 12 mm, Final Packed, Sterile	5301.04.012	FDA UDI	Class II	Active
Klassic Tibial Insert, PS-Post, E-Link	5305.04.011	FDA UDI	Class II	Active
Tibial Insert Trial	2205.01.013	FDA UDI	Class I	Active
Intramedullary Reamer	2014.15.000	FDA UDI	Class I	Active
Screw Pin, Hex Head, 50mm	2706.00.050	FDA UDI	Class I	Active
Tibial Baseplate Trial	2204.03.000	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Max, Std Poly	6300.02.014	FDA UDI	Class II	Active
Rotating Distal Femoral Cut Guide, Klassic ONE	2155.00.000	FDA UDI	Class I	Active
Klassic HD Low Profile Acetabular Insert with XLPE Poly	3510.52.036	FDA UDI	Class II	Active
Hemispherical Acetabular Reamer	1207.48.000	FDA UDI	Class I	Active
Acetabular Cup Sizer	1200.60.000	FDA UDI	Class I	Active
Platform Acetabular Cup Sizer	1225.64.000	FDA UDI	Class I	Active
Klassic Blade Neck Trial, Offset	1111.04.000	FDA UDI	Class I	Active
Femur Trial/Stem Trial Adapter	2800.00.000	FDA UDI	Class I	Active
Klassic Femur, Nonporous	5105.02.000	FDA UDI	Class II	Active
Tibial Insert Trial, PS-Max, Klassic ONE	2252.01.021	FDA UDI	Class I	Active
Femoral Cut Block	2106.07.000	FDA UDI	Class I	Active
Box Chisel	1301.00.000	FDA UDI	Class I	Active
Acetabular Shell with Ti-Coat, 52mm	3400.52.000	FDA UDI	Class II	Active
Stem Trial	2015.16.170	FDA UDI	Class I	Active
Hemispherical Acetabular Reamer	1207.44.000	FDA UDI	Class I	Active
Klassic BiPolar Trial	1340.57.028	FDA UDI	Class I	Active
Femoral Shift Block	2127.00.000	FDA UDI	Class I	Active
Klassic Stem Extension, Cemented	6600.18.120	FDA UDI	Class II	Active
Cone Reamer Guide	2024.00.000	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Post, E-Link Poly	5305.02.021	FDA UDI	Class II	Active
Tibial Sizer	2202.05.000	FDA UDI	Class I	Active
Klassic HD Low Profile Acetabular Insert with XLPE Poly	3510.58.036	FDA UDI	Class II	Active
Cancellous Bone Screw with 6.5mm Head Diameter, 50mm	3600.50.065	FDA UDI	Class II	Active
Tibial Stem Extension Reamer	2209.00.050	FDA UDI	Class I	Active
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 1 , 14mm	5204.01.014	FDA UDI	Class II	Active

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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.

Date	Recall No.	Class	Status	Reason
Sep 23, 2025	Z-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.