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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 13 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Knee Instruments | 02.07.10.3782 | FDA UDI | Class I | Active |
| M.U.S.T. Polyaxial Pedicle Screw | 03.50.075 | EUDAMEDFDA UDI | Class II | Active |
| GMK Primary Total Knee System | 02.07.0410SF | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.79.241 | FDA UDI | Class II | Active |
| Mectalif Posterior | 03.27.034 | FDA UDI | Class II | Active |
| NextAR Platform | 09.23.10.NXDESK | FDA UDI | Class II | Active |
| FairFix Adjustable Button System | 05.05.0134 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 02.23.10.0078 | FDA UDI | Class I | Active |
| Surgical Manual Instrument | 03.22.10.5195 | FDA UDI | Class I | Active |
| Spine Instruments | 03.22.10.2536 | FDA UDI | Class I | Active |
| Spine Instruments | 03.18.10.0070 | FDA UDI | Class I | Active |
| Spine Instruments | 03.75.10.0201 | FDA UDI | Class I | Active |
| Spine Instruments | 03.65.10.0001 | FDA UDI | Class I | Active |
| MectaLIF 3D | 03.43.217 | FDA UDI | Class II | Active |
| MyKnee | 24.1716SM | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 02.18.10.0740 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.2009 | FDA UDI | Class I | Active |
| M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System | 03.65.127 | FDA UDI | Class II | Active |
| M.U.S.T. Rods | 03.50.453 | EUDAMEDFDA UDI | Class II | Active |
| M.U.S.T. Reduction Pedicle Screws | 03.52.714 | EUDAMEDFDA UDI | Class II | Active |
| MectaLIF 3D | 03.43.074 | FDA UDI | Class II | Active |
| Spine Instruments | 03.22.10.3230 | FDA UDI | Class I | Active |
| GMK Sphere Revision System | 02.19.DC04 | FDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.7007 | FDA UDI | Class I | Active |
| M.U.S.T. Pedicle Screw System | 03.77.048 | EUDAMEDFDA UDI | Class II | Active |
| M.U.S.T. MINI Anodized Rod | 03.75.658 | FDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.1303 | FDA UDI | Class I | Active |
| MyKnee | 24.1713M | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.0019 | FDA UDI | Class I | Active |
| Spine Instruments | 03.70.10.0373 | FDA UDI | Class I | Active |
| MySpine Unilateral Guide | 7.1066 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.2056 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.1962 | FDA UDI | Class I | Active |
| Spine Instruments | 03.22.10.1528 | FDA UDI | Class I | Active |
| Mfinity Femoral System | 01.24.10.211 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.2047 | FDA UDI | Class I | Active |
| MectaLIF Anterior System | 03.31.022 | FDA UDI | Class II | Active |
| GMK Sphere Total Knee System | 02.12.0514FR | FDA UDI | Class II | Active |
| HIP Instruments | 01.15.10.2196 | FDA UDI | Class I | Active |
| Mpact Double Mobility Shells | 01.32.146MB | FDA UDI | Class II | Active |
| Evolis Total Knee System | 3046.0216 | FDA UDI | Class II | Active |
| MyKnee | 24.1282S | FDA UDI | Class II | Active |
| MyKnee | 24.1225 | FDA UDI | Class II | Active |
| Spine Instruments | 03.30.10.1810 | FDA UDI | Class I | Active |
| Knee Instruments | 02.77.11.0083 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.2322 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.0723 | FDA UDI | Class I | Active |
| Knee Instruments | 02.18.10.0112 | FDA UDI | Class I | Active |
| MyKnee | 24.3627 | FDA UDI | Class II | Active |
| Knee Instruments | 02.09.10.0172 | FDA UDI | Class I | Active |
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