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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 39 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Femoral Augment, Posterior 6401.06.005
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.44.028
FDA UDI
Class IIActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 58mm 3501.58.036
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.016
FDA UDI
Class IIActive
Distal Hip Reamer, Sz 11 1349.11.000
FDA UDI
Class IActive
Acetabular Cup Positioner, Threaded Shaft 1202.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.011
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.01.018
FDA UDI
Class IActive
Cone Extractor 2023.00.000
FDA UDI
Class IActive
Platform Hooded Acetabular Insert with E-Link 3512.54.036
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.05.011
FDA UDI
Class IIActive
Tibial Insert Trial 2205.04.010
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.41.022
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 36mm Head, Size 52mm 3501.52.036
FDA UDI
Class IIActive
PS-Post Box Trial 2146.03.000
FDA UDI
Class IActive
Klassic Knee Femur, Size 7, Nonporous 5100.07.000
FDA UDI
Class IIActive
Adapter for BIOLOX OPTION Femoral Head, +7mm head length 3301.00.700
FDA UDI
Class IIActive
Klassic Knee Femur, Size 4, Nonporous 5100.04.000
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.58.032
FDA UDI
Class IIActive
Femoral Broach 1100.00.000
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 1, 7mm 5501.01.007
FDA UDI
Class IIActive
Universal Cone Impactor Head, Size 3, 18° 2021.03.018
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6401.01.005
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 3 , 16mm 5203.03.016
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.36.700
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.28.350
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.012
FDA UDI
Class IActive
Klassic Domed Patella with E-Link 5502.02.000
FDA UDI
Class IIActive
Stem Trial 2015.14.040
FDA UDI
Class IActive
Acetabular Insert Trial 1204.58.036
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.010
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert Trial 1226.46.028
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6401.04.005
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.06.011
FDA UDI
Class IIActive
Patella Planer 2305.37.000
FDA UDI
Class IActive
Intramedullary Rod (IM Rod) 2100.00.000
FDA UDI
Class IActive
Femoral Broach 1100.09.000
FDA UDI
Class IActive
Distal Femoral Augment Trial 2810.05.005
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.18.050
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.01.018
FDA UDI
Class IActive
Klassic Knee Sombrero Patella, Size 4, 10mm 5501.04.010
FDA UDI
Class IIActive
Klassic Blade Offset Femoral Stem, Porous, Size 7 3107.07.000
FDA UDI
Class IIActive
Tibial Baseplate Trial 2204.01.000
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 4 3101.04.000
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly, 5302.06.013
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.14.200
FDA UDI
Class IIActive
Klassic BiPolar Head, 58 mm OD, 28 mm Head 3205.58.028
FDA UDI
Class IIActive
Klassic Tibial Augment 6404.03.010
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.01.010
FDA UDI
Class IIActive
Acetabular Insert Trial 1204.54.036
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.