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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 2 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Double Mobility Liner | 01.26.2262MHC | FDA UDI | Class II | Active |
| CoCr Femoral Ball Head | 01.25.032 | FDA UDI | Class II | Active |
| Shoulder System Instrument | 04.01.10.0068 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.0125 | FDA UDI | Class I | Active |
| MUSTmini OC pre-bent Rod | 03.75.624 | FDA UDI | Class II | Active |
| GMK Revision Total Knee System | 02.07.0610SCF | FDA UDI | Class II | Active |
| Spine Instruments | 03.29.10.0408 | FDA UDI | Class I | Active |
| MySpine Unilateral Guide | 7.1064S | FDA UDI | Class II | Active |
| MyKnee | 24.2273M | FDA UDI | Class II | Active |
| MySpine Unilateral Guide | 7.1012S | FDA UDI | Class II | Active |
| SportMeds Instruments | 05.11.10.0042 | FDA UDI | Class I | Active |
| ACDF Stand Alone Cervical | 03.18.728 | FDA UDI | Class II | Active |
| Sports Med Instruments | 05.11.10.0023 | FDA UDI | Class I | Active |
| Sports Med Instruments | 05.13.10.0015 | FDA UDI | Class I | Active |
| Mectalif Posterior Cages | 03.21.124 | FDA UDI | Class II | Active |
| M.U.S.T. Polyaxial Pedicle Screw | 03.50.031 | EUDAMEDFDA UDI | Class II | Active |
| Surgical Manual Instrument | 03.22.10.4116 | FDA UDI | Class I | Active |
| Shoulder Instruments | 04.01.10.0878 | FDA UDI | Class I | Active |
| Hip Instruments | 01.22.10.1181 | FDA UDI | Class I | Active |
| NextAR Spine Platform | 03.57.10.0069 | FDA UDI | Class II | Active |
| MectaLIF 3D | 03.43.099 | FDA UDI | Class II | Active |
| MyKnee PPS | 28.2721 | FDA UDI | Class II | Active |
| MyKnee | 24.2293 | FDA UDI | Class II | Active |
| MectaLIF | 03.27.288 | FDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.0080 | FDA UDI | Class I | Active |
| Masterloc Femoral Stems | 01.39.201 | FDA UDI | Class II | Active |
| Mecta-C Cervical Plate System | 03.70.406 | FDA UDI | Class II | Active |
| Mectalif Posterior | 03.27.046 | FDA UDI | Class II | Active |
| Spine Instruments | 03.52.10.0732 | FDA UDI | Class I | Active |
| MectaLIF | 03.21.235 | FDA UDI | Class II | Active |
| M.U.S.T. Reduction Pedicle Screws | 03.52.732 | EUDAMEDFDA UDI | Class II | Active |
| MectaScrew PEEK | 05.05.0021 | FDA UDI | Class II | Active |
| M.U.S.T. Polyaxial Pedicle Screw | 03.50.036 | EUDAMEDFDA UDI | Class II | Active |
| Knee Instruments | 02.07.10.0291 | FDA UDI | Class I | Active |
| Mecta-C Ti mark | 03.28.116 | FDA UDI | Class II | Active |
| MectaLIF Anterior System | 03.30.043 | FDA UDI | Class II | Active |
| My Knee Femoral Cutting Blocks | 4.2015 | FDA UDI | Class II | Active |
| Bipolar Heads | 25060.2251 | FDA UDI | Class II | Active |
| Spine Instruments | 03.29.10.0430 | FDA UDI | Class I | Active |
| Knee Instrument | 02.12.10.2546 | FDA UDI | Class I | Active |
| NextAR (TM) Shoulder Platform | 04.01.10.1149 | FDA UDI | Class II | Active |
| SportsMed Instruments | 05.05.10.0258 | FDA UDI | Class I | Active |
| Shoulder - TiNbN Coating | 04.01.0264 | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.77.034 | FDA UDI | Class II | Active |
| Shoulder System | 04.01.0227 | FDA UDI | Class II | Active |
| Sports Med Instruments | 05.11.10.0010 | FDA UDI | Class I | Active |
| Shoulder System | 04.01.0157 | FDA UDI | Class II | Active |
| Double Mobility Liner | 01.26.2858M | FDA UDI | Class II | Active |
| M.U.S.T. Monoaxial Pedicle Screw | 03.50.241 | EUDAMEDFDA UDI | Class II | Active |
| MyKnee | 9.2716SM | FDA UDI | Class II | Active |
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