Is this your brand? Sign in to claim ownership.
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
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (24685)
Page 8 of 494| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Double Mobility Liner | 01.26.2852M | FDA UDI | Class II | Active |
| AMIStem H Collared Femoral Stems | 01.18.241 | FDA UDI | Class II | Active |
| Endohead | 01.25.248L | FDA UDI | Class II | Active |
| GMK Hinge and Revision TiNbN coated | 02.09.8TA310 | FDA UDI | Class II | Active |
| GMK Revision Total Knee System | 02.07.2402L | FDA UDI | Class II | Active |
| Hip Instruments | 01.32.10.0074 | FDA UDI | Class I | Active |
| Spine Instruments | 03.30.10.1510 | FDA UDI | Class I | Active |
| M.U.S.T. MINI Anodized Rod | 03.75.617 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 02.18.10.0759 | FDA UDI | Class I | Active |
| MyKnee | 24.1095 | FDA UDI | Class II | Active |
| Surgical Manual Instrument | 03.22.10.5190 | FDA UDI | Class I | Active |
| Surgical Manual Instrument | 02.12.10.8567 | FDA UDI | Class I | Active |
| MectaLIF 3D | 03.43.220 | FDA UDI | Class II | Active |
| MyKnee PPS | 28.2283 | FDA UDI | Class II | Active |
| MyKnee | 24.2286 | FDA UDI | Class II | Active |
| MyKnee | 24.2016SM | FDA UDI | Class II | Active |
| MyKnee | 9.2024 | FDA UDI | Class II | Active |
| Double Mobility Liner | 01.26.2856MHC | FDA UDI | Class II | Active |
| MectaLIF 3D | 03.43.128 | FDA UDI | Class II | Active |
| Spine Instruments | 03.22.10.3548 | FDA UDI | Class I | Active |
| Spine Instruments | 03.22.10.2597 | FDA UDI | Class I | Active |
| NextAR Spine Platform | 03.57.10.0154 | FDA UDI | Class II | Active |
| ACDF Stand Alone Cervical | 03.18.833 | FDA UDI | Class II | Active |
| GMK 3D Metal Tibial Tray | 02.12.3D55R | FDA UDI | Class II | Active |
| MOTO Partial Knee System | 02.18.701RM | FDA UDI | Class II | Active |
| Quadra P femoral stems | 01.12.213 | FDA UDI | Class II | Active |
| Mecta-C Cervical Cages | 03.28.428 | FDA UDI | Class II | Active |
| Hip Instruments | 01.38.10.55620 | FDA UDI | Class I | Active |
| Spine Instruments | 03.51.10.0868 | FDA UDI | Class I | Active |
| MyKnee | 6.2014SM | FDA UDI | Class II | Active |
| GMK Primary Total Knee System | 02.07.2005L | FDA UDI | Class II | Active |
| Knee Instruments | 02.12.10.0331 | FDA UDI | Class I | Active |
| GMK-Revision/Hinge Total Knee System | 02.09.TA115RMLL | FDA UDI | Class II | Active |
| MyKnee NextAR Femur Distal Cutting Block Efficiency | 16.1011 | FDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.3014 | FDA UDI | Class I | Active |
| NextAR Spine Platform | 03.57.10.0175 | FDA UDI | Class II | Active |
| GMK Primary Total Knee System | 02.07.3302R | FDA UDI | Class II | Active |
| Mpact Acetabular System | 01.32.3644HC10A | FDA UDI | Class II | Active |
| GMK-Revision/Hinge Total Knee System | 02.09.0623UCH | FDA UDI | Class II | Active |
| MectaLIF 3D | 03.41.039 | FDA UDI | Class II | Active |
| Spine Instruments | 03.22.10.2301 | FDA UDI | Class I | Active |
| Knee Instruments | 02.07.10.0887 | FDA UDI | Class I | Active |
| MyKnee PPS | 8.2285S | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.61.386 | EUDAMEDFDA UDI | Class II | Active |
| Spine Instruments | 03.51.10.0031 | FDA UDI | Class I | Active |
| Knee Instruments | 02.12.10.0624 | FDA UDI | Class I | Active |
| MyKnee | 6.1713M | FDA UDI | Class II | Active |
| M.U.S.T. Pedicle Screw System | 03.68.323 | EUDAMEDFDA UDI | Class II | Active |
| Knee Instruments | 02.01.10.0066 | FDA UDI | Class I | Active |
| M.U.S.T. Reduction Pedicle Screw | 03.52.703 | EUDAMEDFDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.