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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 20 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MectaLIF | 03.26.220 | FDA UDI | Class II | Active |
| GMK Sphere Total Knee System | 02.12.E0111CRR | FDA UDI | Class II | Active |
| Spine Instruments | 03.29.10.0405 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.8269 | FDA UDI | Class I | Active |
| M.U.S.T. Pedicle Screw System | 03.68.233 | EUDAMEDFDA UDI | Class II | Active |
| Spine Instruments | 03.30.10.2446 | FDA UDI | Class I | Active |
| Shoulder System | 04.01.0121 | FDA UDI | Class II | Active |
| GMK Revision Total Knee System | 02.05.03DW | FDA UDI | Class II | Active |
| Endohead | 01.25.246L | FDA UDI | Class II | Active |
| Versafitcup CC TRIO Acetabular System | 01.26.65.25 | FDA UDI | Class II | Active |
| M.U.S.T. Anodized Rod | 03.50.800 | EUDAMEDFDA UDI | Class II | Active |
| Knee Instruments | 02.09.10.0197 | FDA UDI | Class I | Active |
| MyKnee | 6.3611M | FDA UDI | Class II | Active |
| My Knee Femoral Cutting Blocks MIS | 4.1262 | FDA UDI | Class II | Active |
| Shoulder Instruments | 04.01.10.0355 | FDA UDI | Class I | Active |
| Hip Instruments | 01.37.10.0030 | FDA UDI | Class I | Active |
| M.U.S.T. Rods | 03.52.534 | EUDAMEDFDA UDI | Class II | Active |
| Mpact 3D Metal Acetabular System | 01.38.250 | FDA UDI | Class II | Active |
| Mectalif Oblique | 03.26.035 | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.0235 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.4545 | FDA UDI | Class I | Active |
| Mectalif Oblique | 03.26.005 | FDA UDI | Class II | Active |
| GMK-Revision/Hinge Total Knee System | 02.07.220FDA | FDA UDI | Class II | Active |
| Quadra S femoral stems | 01.12.05SN | FDA UDI | Class II | Active |
| Hip Instruments | 01.38.10.56410 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.0867 | FDA UDI | Class I | Active |
| Spine Instruments | 03.51.10.0601 | FDA UDI | Class I | Active |
| NextAR Spine Platform | 03.57.10.0096 | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.0732 | FDA UDI | Class I | Active |
| HIP Instruments | 01.18.10.070 | FDA UDI | Class I | Active |
| Spine Instruments | 03.30.10.1910 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.5217N | FDA UDI | Class I | Active |
| M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System | 03.67.007 | FDA UDI | Class II | Active |
| MySpine | 7.0716 | FDA UDI | Class II | Active |
| MUST Straight Cross Connector | 03.56.406 | EUDAMEDFDA UDI | Class II | Active |
| Bipolar Heads | 25060.2245 | FDA UDI | Class II | Active |
| M.U.S.T. Polyaxial Pedicle Screw | 03.50.061 | EUDAMEDFDA UDI | Class II | Active |
| GMK Revision Total Knee System | 02.07.0323SCF | FDA UDI | Class II | Active |
| Versafitcup CC TRIO Acetabular System | 01.26.45.0048 | FDA UDI | Class II | Active |
| Double Mobility Liner | 01.26.2248MHC | FDA UDI | Class II | Active |
| Knee Instruments | 02.02.10.0101 | FDA UDI | Class I | Active |
| Knee Instruments | 02.01.10.0038 | FDA UDI | Class I | Active |
| MyKnee | 4.7006S | FDA UDI | Class II | Active |
| Mecta-C Cervical Cages | 03.28.518 | FDA UDI | Class II | Active |
| Mecta-C Cervical Plate System | 03.71.132 | FDA UDI | Class II | Active |
| AMIStem-H Proximal Coating Femoral Stems | 01.18.173 | FDA UDI | Class II | Active |
| Spine Instruments | 03.22.10.0955 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.0080 | FDA UDI | Class I | Active |
| M.U.S.T. Cross Connectors | 03.56.035 | EUDAMEDFDA UDI | Class II | Active |
| M-Vizion Femoral Revision System | 01.22.470 | FDA UDI | Class II | Active |
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