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Sign in to claim this brandWALDEMAR LINK GmbH & Co. KG
US
Last updated May 30, 2026
What WALDEMAR LINK GmbH & Co. KG makes
Waldemar Link GmbH & Co. KG manufactures orthopaedic knee and hip prostheses, including reusable trial implants for the tibia and acetabulum, polyethylene knee and acetabular components, and metallic knee femur stems. Their portfolio also includes positioning instruments for orthopaedic implantations, such as impactors, rasps, and saw guides, as well as knee arthroplasty wedges and dual-mobility acetabular systems.
The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U) and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to regulatory requirements for orthopaedic implants and surgical instruments.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- linkhh.de
- —
- —
- [email protected]
- Phone
- +494053995530
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 315675488
Catalogue (7831)
Page 3 of 157| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LINK Instrument | 165-809/25 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 15-6044/00 | FDA UDI | Class I | Active |
| LINK Instrument | 15-6149/02 | FDA UDI | Class II | Active |
| BiMobile Dual Mobility System - Instruments | 184-321/62 | FDA UDI | Class I | Active |
| Gemini SL | 318-253/12 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-413/12 | FDA UDI | Class II | Active |
| LINK Instruments - Impactors, extractors and insertion | 35-1017/00 | FDA UDI | Class I | Active |
| LinkSymphoKnee | 880-235/24 | FDA UDI | Class II | Active |
| MobileLink Acetabular Cup System | 183-363/36 | FDA UDI | Class II | Active |
| LINK Instruments - Trial implants and size gauges | 16-4367/00 | FDA UDI | Class I | Active |
| MP Reconstruction System - Instruments | 134-500/12 | FDA UDI | Class I | Active |
| Endo-Model Saddle Prosthesis | 15-8007/10 | FDA UDI | Class II | Active |
| SPII Model Lubinus | 127-620/17 | FDA UDI | Class II | Active |
| Endo-Model Knee System - Instruments | 15-3208/08 | FDA UDI | Class I | Active |
| LINK Instruments - Alignment and positioning instruments | 35-1007/00 | FDA UDI | Class I | Active |
| LINK Endo-Model EVO | 15-3950/45 | FDA UDI | Class II | Active |
| MobileLink Acetabular Cup System | 183-376/36 | FDA UDI | Class II | Active |
| Endo-Model SL Knee Prosthesis System | 15-8518/02 | FDA UDI | Class II | Active |
| LINK Instruments - Drills, reamers and saw blades | 130-406/01B | FDA UDI | Class I | Active |
| LinkSymphoKnee - Instruments | 881-253/10 | FDA UDI | Class I | Active |
| LINK Instruments - Trial implants and size gauges | 99-0142/20 | FDA UDI | Class I | Active |
| MobileLink Acetabular Cup System | 183-110/46 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-603/18 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-283/10 | FDA UDI | Class II | Active |
| LINK Instruments - Trial implants and size gauges | 15-6060/01 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 151-106/20 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 151-212/00 | FDA UDI | Class I | Active |
| MobileLink Acetabular Cup System | 183-310/56 | FDA UDI | Class II | Active |
| LINK Instruments - Drills, reamers and saw blades | 16-3204/18 | FDA UDI | Class I | Active |
| LINK Endo-Model EVO | 15-4605/08 | FDA UDI | Class II | Active |
| MP Reconstruction Prosthesis | 172-918/25 | FDA UDI | Class II | Active |
| LINK Instruments - Retractors, bone levers, elevators | 66-3470 | FDA UDI | Class I | Active |
| LINK Instruments - Saw and drill guides | 15-2040/40 | FDA UDI | Class I | Active |
| SPII Model Lubinus | 127-933/26 | FDA UDI | Class II | Active |
| Endo-Model Knee System - Instruments | 151-915/00 | FDA UDI | Class I | Active |
| Gemini SL | 318-254/14 | FDA UDI | Class II | Active |
| LINK Endo-Model EVO | 15-4305/08 | FDA UDI | Class II | Active |
| Endo-Model Standard Knee Prosthesis System | 15-3027/13 | FDA UDI | Class II | Active |
| Endo-Model Knee System - Instruments | 16-0118/01 | FDA UDI | Class I | Active |
| LINK Endo-Model EVO | 15-4620/12 | FDA UDI | Class II | Active |
| LINK Endo-Model EVO | 15-3950/23 | FDA UDI | Class II | Active |
| Endo-Model Knee System - Instruments | 15-3209/14 | FDA UDI | Class I | Active |
| LINK Instrument | 319-220/00 | FDA UDI | Class II | Active |
| BiMobile Dual Mobility System - Instruments | 131-170/51 | FDA UDI | Class I | Active |
| LINK Embrace Shoulder System | 643-242/13 | FDA UDI | Class II | Active |
| TrabecuLink Femoral and Tibial Cone - Instruments | 15-6124/04 | FDA UDI | Class I | Active |
| LINK Endo-Model EVO | 15-2951/56 | FDA UDI | Class II | Active |
| Endo-Model SL Knee Prosthesis System | 15-8527/40 | FDA UDI | Class II | Active |
| Vario-Cup System | 107-230/57 | FDA UDI | Class II | Active |
| Gemini SL | 318-102/26 | FDA UDI | Class II | Active |
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