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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
—
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 24 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Knee Tibial Insert, CR/Congruent, Size 4, 18 mm, Final Packed, Sterile 5300.04.018
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 54mm 3502.54.032
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 5 , 14mm 5204.05.014
FDA UDI
Class IIActive
Acetabular Insert Impactor 1205.32.000
FDA UDI
Class IActive
Tibial Broach Stem 2203.00.050
FDA UDI
Class IActive
Klassic BiPolar Sizing Handle 1323.28.000
FDA UDI
Class IActive
Klassic Blade Neck Trial, Offset 1111.01.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.54.028
FDA UDI
Class IActive
Acetabular Insert with E-Link Poly, 36mm Head, Size 60mm 3502.60.036
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.18.040
FDA UDI
Class IIActive
28mm BIOLOX delta Ceramic Femoral Head, 12/14 taper 3203.28.035
FDA UDI
Class IIActive
Modular Reamer Driver 2150.00.000
FDA UDI
Class IActive
Klassic Femur with Cobalt 3D, size 3 5102.03.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, CR/Congruent, Size 5, 18 mm, Final Packed, Sterile 5300.05.018
FDA UDI
Class IIActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.01.000
FDA UDI
Class IActive
Klassic Knee Femur, Revision 6100.02.000
FDA UDI
Class IIActive
Klassic Blade Femoral Broach 1109.09.000
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 48mm 3503.48.032
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 58mm 3502.58.032
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 4 , 12mm 5204.04.012
FDA UDI
Class IIActive
Hemispherical Acetabular Reamer 1207.51.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.52.036
FDA UDI
Class IIActive
Klassic Knee Tibial Baseplate Assembly, Size 5 5200.05.000
FDA UDI
Class IIActive
Femoral Broach 1100.08.000
FDA UDI
Class IActive
Femoral Cut Block, Narrow 2139.01.000
FDA UDI
Class IActive
Tibial Stem Extension Reamer 2209.00.025
FDA UDI
Class IActive
Klassic Blade Femoral Broach 1109.03.000
FDA UDI
Class IActive
Universal Cone Impactor Head, Size 1, 12° 2021.01.012
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.013
FDA UDI
Class IIActive
Klassic Tibial Baseplate, Revision 6200.01.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.05.005
FDA UDI
Class IIActive
Platform Acetabular Cup Sizer 1225.52.000
FDA UDI
Class IActive
MIS Tibial Cut Block - Right 2218.00.000
FDA UDI
Class IActive
32mm Femoral Head, 12/14 Taper, -3.5mm Offset 3200.32.035
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.021
FDA UDI
Class IIActive
Tibial Broach Guide, Klassic ONE 2236.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.014
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 2 , 14mm 5204.02.014
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.012
FDA UDI
Class IActive
Klassic BiPolar Sizing Handle, Locking 1341.22.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.01.016
FDA UDI
Class IActive
Klassic HD Hip Offset Femoral Stem Trial 1316.08.000
FDA UDI
Class IActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 5 5201.05.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 43 mm OD, 22 mm Head 3205.43.022
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.024
FDA UDI
Class IIActive
32mm BIOLOX OPTION Femoral Head, 16/18 taper 3204.32.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.024
FDA UDI
Class IIActive
32mm BIOLOX delta Femoral Head, 12/14 taper, -3.5mm Head Length 3203.32.035
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.02.018
FDA UDI
Class IActive
Femoral Trial, PS-Post/Revision 2126.05.000
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.