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Sign in to claim this brandTOTAL JOINT ORTHOPEDICS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1567 E. Stratford Avenue, Salt Lake City, UT, 84106
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3008544874
- DUNS Number
- —
Catalogue (2063)
Page 14 of 42| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hooded Acetabular Insert Trial | 1223.62.032 | FDA UDI | Class I | Active |
| Tibial Baseplate Trial, Pegless | 2204.01.200 | FDA UDI | Class I | Active |
| Tibial Alignment Guide - 0 degree Spiked Upper Tower, Klassic ONE | 2256.00.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, Ultra-PS, E-Link Poly | 5303.01.016 | FDA UDI | Class II | Active |
| Klassic HD Hip Offset Femoral Stem Trial | 1316.07.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, E-Link | 5305.04.016 | FDA UDI | Class II | Active |
| Klassic Femur with Cobalt 3D | 5106.04.000 | FDA UDI | Class II | Active |
| Stem Trial | 2015.16.200 | FDA UDI | Class I | Active |
| Sombrero Patella Trial | 2307.04.010 | FDA UDI | Class I | Active |
| Klassic BiPolar Trial | 1340.54.028 | FDA UDI | Class I | Active |
| Klassic Femoral Augment, Posterior | 6400.03.010 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, Std Poly | 5304.05.014 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, E-Link Poly | 5305.05.018 | FDA UDI | Class II | Active |
| Klassic Knee Tibial Insert, CR/Congruent, Size 6, 14 mm, Final Packed, Sterile | 5300.06.014 | FDA UDI | Class II | Active |
| PS-Post Box Trial, Klassic ONE | 2165.01.000 | FDA UDI | Class I | Active |
| Platform Acetabular Cup with Ti-Coat | 3401.62.000 | FDA UDI | Class II | Active |
| Klassic HD Hooded Acetabular Insert with E-Link Poly | 3507.62.036 | FDA UDI | Class II | Active |
| Femoral Head Trial | 1306.36.000 | FDA UDI | Class I | Active |
| Stem Trial | 2015.13.070 | FDA UDI | Class I | Active |
| Modular Knee Impactor Head, Femur | 2130.00.000 | FDA UDI | Class I | Active |
| Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 2 , 12mm | 5203.02.012 | FDA UDI | Class II | Active |
| Tibial Insert Trial, Klassic ONE | 2240.04.016 | FDA UDI | Class I | Active |
| Klassic Blade Neck Trial, Offset | 1111.03.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, Std Poly | 5304.03.013 | FDA UDI | Class II | Active |
| Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 1 , 10mm | 5204.01.010 | FDA UDI | Class II | Active |
| Klassic Femoral Head Trial | 1346.22.000 | FDA UDI | Class I | Active |
| Stem Trial | 2015.20.120 | FDA UDI | Class I | Active |
| Stem Trial | 2015.15.150 | FDA UDI | Class I | Active |
| Klassic Femur, Nonporous | 5105.06.000 | FDA UDI | Class II | Active |
| Klassic Femoral Head Trial | 1346.22.200 | FDA UDI | Class I | Active |
| Klassic BiPolar Trial | 1340.46.028 | FDA UDI | Class I | Active |
| Klassic Femoral Augment, Distal | 6402.01.005 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.02.012 | FDA UDI | Class I | Active |
| Drill and Pin Set, Smooth | 2703.00.000 | FDA UDI | Class I | Active |
| Klassic Femur, PS-Post | 5101.07.000 | FDA UDI | Class II | Active |
| Klassic Femur with Cobalt 3D | 5106.05.000 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, CR/Congruent, E-Link Poly | 5302.03.018 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, E-Link | 5305.01.016 | FDA UDI | Class II | Active |
| Femoral Trial, PS-Post/Revision, Klassic ONE | 2170.01.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post | 2224.04.013 | FDA UDI | Class I | Active |
| Bent Retractor | 2002.00.000 | FDA UDI | Class I | Active |
| Stem Trial | 2015.14.070 | FDA UDI | Class I | Active |
| Klassic Stem Extension, Cemented | 6600.10.040 | FDA UDI | Class II | Active |
| Tibial Stylus, Klassic ONE | 2242.00.000 | FDA UDI | Class I | Active |
| Drill and Pin Set, Smooth, Non-Sterile | 2604.00.001 | FDA UDI | Class I | Active |
| Tibial Broach | 2203.03.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post | 2224.02.014 | FDA UDI | Class I | Active |
| Slap Hammer | 1304.00.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Max, Std Poly | 6300.02.016 | FDA UDI | Class II | Active |
| Fixed Distal Femoral Cut Guide, Klassic ONE | 2156.00.004 | FDA UDI | Class I | Active |
Related Companies
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 23, 2025 | Z-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. |