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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 17 of 42| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tibial Insert Trial | 2205.05.010 | FDA UDI | Class I | Active |
| Tibial Insert Trial | 2205.06.010 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post | 2224.05.021 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.05.014 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.01.018 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post, Klassic ONE | 2254.03.021 | FDA UDI | Class I | Active |
| Randell Impactor | SRI-10031 | FDA UDI | Class I | Active |
| Stem Trial | 2015.15.040 | FDA UDI | Class I | Active |
| Klassic HD Hooded Acetabular Insert with XLPE Poly | 3508.58.036 | FDA UDI | Class II | Active |
| Tibial Baseplate Trial, Flat | 2204.06.100 | FDA UDI | Class I | Active |
| Intramedullary Reamer, Revision | 2026.12.000 | FDA UDI | Class I | Active |
| Universal Cone Impactor Head | 2021.57.024 | FDA UDI | Class I | Active |
| Hooded Acetabular Insert Trial | 1223.52.036 | FDA UDI | Class I | Active |
| PS-Post Box Trial | 2146.05.000 | FDA UDI | Class I | Active |
| Stem Trial | 2015.18.100 | FDA UDI | Class I | Active |
| Klassic HD Modular Femoral Broach | 1106.08.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial | 2205.03.014 | FDA UDI | Class I | Active |
| Klassic Blade Neck Trial, Offset | 1111.02.000 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Post | 2224.01.018 | FDA UDI | Class I | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.02.022 | FDA UDI | Class I | Active |
| Simple Gap Block, Straight | 2222.05.014 | FDA UDI | Class I | Active |
| Tibial Alignment Guide, 0 upper tower | 2231.00.000 | FDA UDI | Class I | Active |
| Acetabular Insert with E-Link Poly, 36mm Head, Size 58mm | 3502.58.036 | FDA UDI | Class II | Active |
| Cone Reamer Guide | 2024.00.100 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, E-Link Poly | 5305.06.021 | FDA UDI | Class II | Active |
| Klassic ONE, CR/Ultra-PS, PS-Post Conversion Instrumentation Tray | 2413.00.000 | FDA UDI | Class I | Active |
| Femoral Trial | 2108.01.000 | FDA UDI | Class I | Active |
| Femur Impactor Head | 2115.00.400 | FDA UDI | Class I | Active |
| Acetabular Cup Sizer | 1200.54.000 | FDA UDI | Class I | Active |
| Platform Neutral Acetabular Insert Trial | 1226.52.036 | FDA UDI | Class I | Active |
| Femoral Trial, PS-Post/Revision, Klassic ONE | 2170.04.000 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Max, Std Poly | 6300.05.021 | FDA UDI | Class II | Active |
| Klassic Stem Extension, Femoral, Cemented | 6600.14.120 | FDA UDI | Class II | Active |
| Tibial Insert Trial, PS-Max, Klassic ONE | 2252.04.011 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, E-Link | 5305.02.013 | FDA UDI | Class II | Active |
| Klassic HD Hooded Acetabular Insert with E-Link Poly | 3507.54.032 | FDA UDI | Class II | Active |
| Klassic BiPolar Trial | 1340.56.028 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, CR/Congruent, E-Link Poly | 5302.01.012 | FDA UDI | Class II | Active |
| Patella Trial | 2303.04.000 | FDA UDI | Class I | Active |
| Femoral Trial, PS-Post/Revision | 2126.01.000 | FDA UDI | Class I | Active |
| Klassic BiPolar Trial | 1340.59.028 | FDA UDI | Class I | Active |
| Klassic Tibial Insert, PS-Post, E-Link Poly | 5305.04.021 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, Ultra-PS, E-Link Poly | 5303.04.011 | FDA UDI | Class II | Active |
| Stem Trial | 2015.17.070 | FDA UDI | Class I | Active |
| Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 2 , 14mm | 5203.02.014 | FDA UDI | Class II | Active |
| Universal Handle | 2107.00.000 | FDA UDI | Class I | Active |
| Klassic Tibial Baseplate, Revision | 6201.01.000 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, Std Poly | 5304.05.011 | FDA UDI | Class II | Active |
| Klassic Tibial Augment & Screw | 6405.05.010 | FDA UDI | Class II | Active |
| Klassic Tibial Insert, PS-Post, Std Poly | 5304.05.018 | FDA UDI | Class II | Active |
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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. |