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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 3 of 42| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.06.014 | FDA UDI | Class I | Active |
| Universal Impactor Head | 2219.00.000 | FDA UDI | Class I | Active |
| Klassic Knee Tibial Baseplate Assembly, Size 1 | 5200.01.000 | FDA UDI | Class II | Active |
| Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 5 , 16mm | 5204.05.016 | FDA UDI | Class II | Active |
| Klassic Stem Extension, Cemented | 6600.12.040 | FDA UDI | Class II | Active |
| BiPolar Femoral Head Trial | 1326.28.700 | FDA UDI | Class I | Active |
| Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 6 , 16mm | 5203.06.016 | FDA UDI | Class II | Active |
| Klassic Tibial Augment | 6404.05.010 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, E-Link Poly | 5305.06.024 | FDA UDI | Class II | Active |
| Klassic Tibial Augment | 6404.01.010 | FDA UDI | Class II | Active |
| Klassic Sombrero Patella with E-Link | 5503.01.007 | FDA UDI | Class II | Active |
| Klassic HD Low Profile Acetabular Insert with E-Link Poly | 3509.64.036 | FDA UDI | Class II | Active |
| Platform Hooded Acetabular Insert with E-Link | 3512.46.028 | FDA UDI | Class II | Active |
| Klassic BiPolar Trial | 1322.46.028 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, E-Link | 5305.06.010 | FDA UDI | Class II | Active |
| Klassic Femur, PS-Post | 5101.03.000 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, E-Link Poly | 5305.02.024 | FDA UDI | Class II | Active |
| Femoral Trial | 2108.02.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post | 2224.01.011 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.03.022 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Max, Std Poly | 6300.06.016 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.03.012 | FDA UDI | Class I | Active |
| MIS Cut Block Modified, Right | SRI-10039 | FDA UDI | Class I | Active |
| 36mm BIOLOX OPTION Femoral Head, 16/18 taper | 3204.36.000 | FDA UDI | Class II | Active |
| BIOLOX CONTOURA Ceramic Femoral Head | 3206.32.700 | FDA UDI | Class II | Active |
| Contoura Femoral Head Trial | 1347.36.350 | FDA UDI | Class I | Active |
| Klassic Femoral Augment, Distal | 6402.05.010 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.05.013 | FDA UDI | Class I | Active |
| Hooded Acetabular Insert Trial | 1223.58.036 | FDA UDI | Class I | Active |
| Femur Trial | 2147.01.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, Std Poly | 5304.03.024 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.02.024 | FDA UDI | Class I | Active |
| Acetabular Cup Sizer | 1200.44.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Max, Std Poly | 6300.02.022 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Max, Std Poly | 6300.03.013 | FDA UDI | Class II | Active |
| Klassic BiPolar Trial | 1340.60.028 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, CR/Congruent, E-Link Poly | 5302.02.011 | FDA UDI | Class II | Active |
| Klassic Femoral Augment, Distal | 6403.01.005 | FDA UDI | Class II | Active |
| Stem Trial | 2015.14.170 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, CR/Congruent, E-Link Poly | 5302.02.012 | FDA UDI | Class II | Active |
| Klassic Knee Tibial Insert, Ultra-PS, Size 2, 18 mm, Final Packed, Sterile | 5301.02.018 | FDA UDI | Class II | Active |
| Klassic BiPolar Trial | 1322.60.028 | FDA UDI | Class I | Active |
| Klassic Femur, Nonporous | 5105.05.000 | FDA UDI | Class II | Active |
| Stem Trial | 2015.18.070 | FDA UDI | Class I | Active |
| Femoral Trial, PS-Post/Revision | 2126.06.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial | 2205.05.018 | FDA UDI | Class I | Active |
| Acetabular Cup Sizer | 1200.62.000 | FDA UDI | Class I | Active |
| Acetabular Cup Sizer | 1200.58.000 | FDA UDI | Class I | Active |
| Universal Cone | 6800.07.024 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.01.010 | FDA UDI | Class I | Active |
Related Companies
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Importers
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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. |