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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 31 of 42
DeviceModel / ReferenceRegistriesClassStatus
Tibial Insert Trial, Klassic ONE 2240.03.016
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.04.013
FDA UDI
Class IActive
Acetabular U-Joint Screwdriver 1210.00.000
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.02.010
FDA UDI
Class IActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.07.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.04.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.05.024
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.022
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.05.014
FDA UDI
Class IIActive
Acetabular Reamer Adapter SRI-10044
FDA UDI
Class IActive
Klassic BiPolar Head, 46 mm OD, 28 mm Head 3205.46.028
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.06.018
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.03.013
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.02.020
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.32.000
FDA UDI
Class IActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 5 3103.05.000
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.04.018
FDA UDI
Class IActive
MIS Tibial Cut Block - Left 2217.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.01.018
FDA UDI
Class IIActive
Universal Cone Trial, Size 3, 18° 2022.03.018
FDA UDI
Class IActive
Tibial Insert Trial 2205.01.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.01.013
FDA UDI
Class IActive
22mm BIOLOX delta Ceramic Femoral Head, 12/14 taper 3203.22.000
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.020
FDA UDI
Class IActive
Sombrero Patella Trial 2307.02.007
FDA UDI
Class IActive
Drill and Pin Set, Sharp 2704.00.000
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.53.000
FDA UDI
Class IActive
Platform Neutral Acetabular Insert with E-Link 3511.48.032
FDA UDI
Class IIActive
Klassic Tibial Baseplate for Primary or Revision, Nonporous, size 1 5201.01.000
FDA UDI
Class IIActive
Hooded Acetabular Insert Trial 1223.50.032
FDA UDI
Class IActive
Klassic Femur with Cobalt 3D 5106.06.000
FDA UDI
Class IIActive
Klassic HD Acetabular Cup with Ti-Coat 3400.46.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6403.06.005
FDA UDI
Class IIActive
Anterior Starter Broach 1115.00.000
FDA UDI
Class IActive
Stem Trial 2015.16.040
FDA UDI
Class IActive
Klassic Femoral Head Trial 1346.28.700
FDA UDI
Class IActive
Platform Neutral Acetabular Insert with E-Link 3511.52.036
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.011
FDA UDI
Class IIActive
Tibial Baseplate Trial, Flat 2204.04.100
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.60.036
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 5 , 14mm 5203.05.014
FDA UDI
Class IIActive
Acetabular Reamer Driver, Straight 1208.00.000
FDA UDI
Class IActive
Klassic ONE Universal Cone & Revision Baseplate Tray, Baseplate Insert 2417.00.200
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.06.024
FDA UDI
Class IActive
Intramedullary Rod, Klassic ONE 2162.00.000
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.02.018
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.05.016
FDA UDI
Class IActive
Klassic Knee Case 2, Tibial Preparation Instrumentation 2402.00.000
FDA UDI
Class IActive
PS-Post Box Resection Guide 2145.01.000
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 3 , 12mm 5204.03.012
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.