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Sign in to claim this brandMedacta International
US
Last updated May 23, 2026
What Medacta International makes
Medacta International manufactures orthopaedic surgical instruments and implants, including reusable surgical procedure kits, single-use positioning instruments, spinal bone screws, spinal interbody fusion cages, tibial inserts, acetabular liners, shoulder prostheses, and knee inserts.
The company's portfolio includes Class I and Class II devices listed in the FDA UDI registry, and they are based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Medacta International manufacture?
Medacta International manufactures orthopaedic surgical instruments and implants, including reusable surgical procedure kits, single-use positioning instruments, spinal bone screws, spinal interbody fusion cages, tibial inserts, acetabular liners, shoulder prostheses, and knee inserts.
Where is Medacta International based?
Medacta International is based in the US, as indicated in the provided device data.
Which registries list Medacta International's devices?
Medacta International's devices are listed in the FDA UDI registry, as specified in the device data.
How are Medacta International's devices classified?
Medacta International's devices are classified as Class I and Class II, as indicated in the provided device data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (24685)
Page 10 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MyKnee | 6.1716M | FDA UDI | Class II | Active |
| MyKnee PPS | 28.2017 | FDA UDI | Class II | Active |
| MyKnee | 24.2296 | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.0115 | FDA UDI | Class I | Active |
| ACDF Stand Alone Cervical | 03.18.509 | FDA UDI | Class II | Active |
| MectaLIF Anterior System | 03.31.018 | FDA UDI | Class II | Active |
| GMK Revision Total Knee System | 02.07.0320PSE | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.68.807 | EUDAMEDFDA UDI | Class II | Active |
| Mecta-C Cervical Plate System | 03.70.148 | FDA UDI | Class II | Active |
| MyKnee LBS | 4.1661 | FDA UDI | Class II | Active |
| GMK Uni | 02.08.IF5.09.RMLL | FDA UDI | Class II | Active |
| GMK Primary Total Knee System | 02.07.2206L | FDA UDI | Class II | Active |
| Hip Instruments | 01.32.10.0381 | FDA UDI | Class I | Active |
| MectaLIF | 03.27.282 | FDA UDI | Class II | Active |
| Spine Instruments | 03.22.10.3588 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.9727 | FDA UDI | Class I | Active |
| Knee Instruments | 02.02.10.0211 | FDA UDI | Class I | Active |
| M-Vizion Femoral Revision System | 01.22.511 | FDA UDI | Class II | Active |
| HIP Instruments | 01.22.10.0664 | FDA UDI | Class I | Active |
| M.U.S.T. Pedicle Screw System | 03.62.113 | EUDAMEDFDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.7027 | FDA UDI | Class I | Active |
| GMK Sphere Total Knee System | 02.12.E0210CRL | FDA UDI | Class II | Active |
| M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System | 03.65.655 | FDA UDI | Class II | Active |
| Hip instrument | 01.18.10.461 | FDA UDI | Class I | Active |
| MyKnee | 24.1725M | FDA UDI | Class II | Active |
| GMK Sphere Total Knee System | 02.12.E0612FL | FDA UDI | Class II | Active |
| Quadra P femoral stems | 01.12.278 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 03.22.10.4132 | FDA UDI | Class I | Active |
| MyKnee | 24.1767 | FDA UDI | Class II | Active |
| MyKnee | 24.2073SM | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.68.264 | EUDAMEDFDA UDI | Class II | Active |
| MyKnee | 24.2017 | FDA UDI | Class II | Active |
| Knee Instruments | 02.18.10.0256 | FDA UDI | Class I | Active |
| Surgical Manual Instrument | 03.22.10.4109 | FDA UDI | Class I | Active |
| Shoulder Instruments | 04.01.10.0626 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.4079 | FDA UDI | Class I | Active |
| Mecta-C Ti mark | 03.28.124 | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.57.241 | FDA UDI | Class II | Active |
| MiniMAX Stems | 01.13.107L | FDA UDI | Class II | Active |
| Quadra R femoral stems | 01.12.060 | FDA UDI | Class II | Active |
| Versacem Acetabular Shell and Double Mobility HC Liners | 01.26.2846MHC | FDA UDI | Class II | Active |
| SnugFit All-Suture Anchor | 05.11.021 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 02.18.10.5078 | FDA UDI | Class I | Active |
| Spine Instruments | 03.51.10.0105 | FDA UDI | Class I | Active |
| Surgical Manual Instrument | 03.22.10.5084 | FDA UDI | Class I | Active |
| MectaLIF 3D | 03.43.042 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.3006 | FDA UDI | Class I | Active |
| HIP Instruments | 01.18.10.1715 | FDA UDI | Class I | Active |
| Hip Instruments | 01.22.10.0160 | FDA UDI | Class I | Active |
| GMK Total Knee System | 02.12.KA55L | FDA UDI | Class II | Active |
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