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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 20 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Tibial Insert, PS-Post, E-Link 5305.01.012
FDA UDI
Class IIActive
Modular Liner Impactor Head 1222.22.000
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem, Porous, Size 8 3107.08.000
FDA UDI
Class IIActive
Alignment Rod, Klassic ONE 2168.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.013
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.05.011
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6402.03.010
FDA UDI
Class IIActive
Platform Acetabular Cup with Ti-Coat 3401.52.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 53 mm OD, 28 mm Head 3205.53.028
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.01.011
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.01.010
FDA UDI
Class IActive
Modular Femoral Head Trial 1326.36.700
FDA UDI
Class IActive
Klassic Stem Extension, Cemented 6600.16.040
FDA UDI
Class IIActive
Klassic Femoral Head Trial 1346.32.700
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.06.021
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.016
FDA UDI
Class IIActive
3.2mm Drill Tip 1219.25.032
FDA UDI
Class IActive
Sombrero Patella Trial 2307.01.010
FDA UDI
Class IActive
Klassic HD Hip Case 2, Acetabular Instruments 1406.00.000
FDA UDI
Class IActive
Klassic HD Hip Offset Femoral Stem Trial 1316.03.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.03.016
FDA UDI
Class IActive
Hemispherical Acetabular Reamer 1207.56.000
FDA UDI
Class IActive
Stem Trial 2015.20.200
FDA UDI
Class IActive
Tibial Broach 2203.05.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.48.032
FDA UDI
Class IIActive
Stem Trial 2015.13.150
FDA UDI
Class IActive
Klassic Knee Tibial Set Screw 5602.00.000
FDA UDI
Class IIActive
Klassic HD Hip System Offset Femoral Stem, Porous, size 8 3103.08.000
FDA UDI
Class IIActive
Quick Pin, Smooth 2004.30.100
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.020
FDA UDI
Class IIActive
Tibial Insert Trial, Klassic ONE 2240.05.010
FDA UDI
Class IActive
Femoral Cut Block, Narrow 2139.06.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.49.028
FDA UDI
Class IActive
Platform Hooded Acetabular Insert Trial 1228.56.036
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.03.014
FDA UDI
Class IIActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.50.032
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.05.024
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegless 2204.04.200
FDA UDI
Class IActive
All-Poly Tibial Broach, Klassic ONE 2245.03.000
FDA UDI
Class IActive
Femur Trial 2147.02.000
FDA UDI
Class IActive
Klassic HD Hip Offset Femoral Stem Trial 1316.02.000
FDA UDI
Class IActive
Tibial Insert Assembly Clamp 2208.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.018
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.021
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.012
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D, size 4 5102.04.000
FDA UDI
Class IIActive
Klassic Femoral Augment Screw, Distal 6407.00.005
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 36mm Head, Size 52mm 3502.52.036
FDA UDI
Class IIActive
Curved Acetabular Cup Impactor – Ball Hex Driver 1214.00.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.52.036
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.