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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 8 of 42
DeviceModel / ReferenceRegistriesClassStatus
22mm BIOLOX delta Ceramic Femoral Head, 12/14 taper 3203.22.200
FDA UDI
Class IIActive
Universal Cone Reamer, Basket, Size 5-7, 24° 2020.05.024
FDA UDI
Class IActive
Adapter for BIOLOX OPTION Femoral Head, -3.5mm head length 3301.00.035
FDA UDI
Class IIActive
Tibial Baseplate Trial, Pegless 2204.06.200
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.54.036
FDA UDI
Class IActive
Klassic Blade Femoral Stem Impactor, Ball Tip 1328.00.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 5, 10 mm, Final Packed, Sterile 5300.05.010
FDA UDI
Class IIActive
Distal Femoral Augment Trial 2810.03.005
FDA UDI
Class IActive
Stem Trial 2015.13.040
FDA UDI
Class IActive
Klassic HD Hip Case 2, Acetabular Preparation Instruments 1402.00.000
FDA UDI
Class IActive
Universal Cone Impactor Head 2021.12.012
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.016
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.16.000
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 9 3101.09.000
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.01.012
FDA UDI
Class IActive
Femoral Trial 2108.04.000
FDA UDI
Class IActive
Klassic Tibial Augment & Screw 6405.01.010
FDA UDI
Class IIActive
Spline Wrench Handle Cover 2018.00.100
FDA UDI
Class IActive
Femoral Cut Block, Narrow 2139.05.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 4 , 10mm 5203.04.010
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.04.010
FDA UDI
Class IIActive
Patella Cement Clamp, Klassic ONE, Tip 2312.00.000
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.54.000
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.10.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 2 , 10mm 5203.02.010
FDA UDI
Class IIActive
Klassic Blade Femoral Stem, Porous, Size 5 3105.05.000
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 4 3103.04.000
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.14.070
FDA UDI
Class IIActive
Klassic Femur with Aurum 5104.06.000
FDA UDI
Class IIActive
Patella Trial 2303.02.000
FDA UDI
Class IActive
Klassic Tibial Baseplate, Revision 6200.04.000
FDA UDI
Class IIActive
Distal Femoral Augment Trial 2810.01.010
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.02.008
FDA UDI
Class IActive
All-Poly Tibial Impactor Head 2220.00.000
FDA UDI
Class IActive
Hex Screwdriver 2206.00.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.52.032
FDA UDI
Class IIActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 3 3101.03.000
FDA UDI
Class IIActive
PS-Post Instrument Tray 2410.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.011
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.018
FDA UDI
Class IIActive
BIOLOX CONTOURA Ceramic Femoral Head 3206.28.350
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.010
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.28.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 62mm 3503.62.032
FDA UDI
Class IIActive
Klassic BiPolar Head, 42 mm OD, 22 mm Head 3205.42.022
FDA UDI
Class IIActive
Klassic Blade Femoral Broach 1109.11.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.58.036
FDA UDI
Class IIActive
Hemispherical Acetabular Reamer 1207.59.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 64mm 3503.64.036
FDA UDI
Class IIActive
Cancellous Bone Screw with 6.5mm Head Diameter, 40mm 3600.40.065
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.