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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 19 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Spine Instruments | 03.52.10.0731 | FDA UDI | Class I | Active |
| Spine Instruments | 03.51.10.7204 | FDA UDI | Class I | Active |
| NextAR Spine Platform | 03.57.10.0110 | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.63.321 | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.77.050 | EUDAMEDFDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screws System | 03.68.570 | EUDAMEDFDA UDI | Class II | Active |
| Surgical Manual Instrument | 03.22.10.5003 | FDA UDI | Class I | Active |
| MyKnee | 24.3661 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 11.01317 | FDA UDI | Class I | Active |
| Hip Instruments | 01.37.10.0081 | FDA UDI | Class I | Active |
| MySpine Unilateral Guide | 7.1005S | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.4726 | FDA UDI | Class I | Active |
| M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System | 03.65.323 | FDA UDI | Class II | Active |
| MUSTmini Occipital screw | 03.75.822 | FDA UDI | Class II | Active |
| Hip Instruments | 01.32.10.1560 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.0434 | FDA UDI | Class I | Active |
| GMK Sphere Total Knee System | 02.12.0613FR | FDA UDI | Class II | Active |
| GMK Sphere Total Knee System | 02.12.0420CL | FDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.0371 | FDA UDI | Class I | Active |
| Hip Instruments | 01.10.10.404 | FDA UDI | Class I | Active |
| M-Vizion Femoral Revision System | 01.22.169 | FDA UDI | Class II | Active |
| MectaLIF | 03.27.157 | FDA UDI | Class II | Active |
| M.U.S.T. Reduction Pedicle Screws | 03.52.711 | FDA UDI | Class II | Active |
| MectaLIF | 03.26.207 | FDA UDI | Class II | Active |
| HIP Instruments | 01.39.10.0034 | FDA UDI | Class I | Active |
| My Spine Pedicle Screw Placement Guides | 7.0050 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.1083 | FDA UDI | Class I | Active |
| Shoulder Instruments | 04.01.10.0396 | FDA UDI | Class I | Active |
| GMK Sphere Total Knee System | 02.12.0514FL | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.4707 | FDA UDI | Class I | Active |
| Hip Instruments | 01.32.10.0006 | FDA UDI | Class I | Active |
| ACDF Stand Alone Cervical | 03.18.714 | FDA UDI | Class II | Active |
| M.U.S.T. MINI Polyaxial Screw | 03.75.109 | FDA UDI | Class II | Active |
| Evolis Total Knee System | 3042.0316 | FDA UDI | Class II | Active |
| Mectalif Transforaminal Cages TiPEEK | 03.23.152 | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.4891 | FDA UDI | Class I | Active |
| MectaLock All-Suture Anchor | 05.11.015 | FDA UDI | Class II | Active |
| MectaLIF | 03.26.263 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.0966 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.3583 | FDA UDI | Class I | Active |
| Hip Instruments | 01.10.10.376 | FDA UDI | Class I | Active |
| Shoulder System | 04.01.0210 | FDA UDI | Class II | Active |
| Mecta-C Ti mark | 03.28.209 | FDA UDI | Class II | Active |
| GMK Sphere Total Knee System | 02.12.0021R | FDA UDI | Class II | Active |
| Knee Instruments | 11.01053 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.1966 | FDA UDI | Class I | Active |
| MySpine Unilateral Guide | 7.1031 | FDA UDI | Class II | Active |
| Knee Instruments | 33.22.0134 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.1058 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.1908 | FDA UDI | Class I | Active |
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