Is this your brand? Sign in to claim ownership.
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 1 of 157| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LINK Instruments - Impactors, extractors and insertion | 15-2040/06 | FDA UDI | Class I | Active |
| LINK Instrument | 317-810/14 | FDA UDI | Class II | Active |
| LINK Endo-Model EVO Knee System | 15-2951/97 | FDA UDI | Class II | Active |
| LINK Instruments - Trial implants and size gauges | 16-4161/16 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 151-206/02 | FDA UDI | Class I | Active |
| Gemini SL | 318-113/26 | FDA UDI | Class II | Active |
| BiMobile Dual Mobility System - Instruments | 184-352/50 | FDA UDI | Class II | Active |
| MobileLink Acetabular Cup System | 183-850/28 | FDA UDI | Class II | Active |
| Endo-Model Knee System - Instruments | 151-616/12 | FDA UDI | Class I | Active |
| LINK Instruments - Saw and drill guides | 340-034 | FDA UDI | Class I | Active |
| LINK Instruments - Rasps, compressors and broaches | 319-260/00 | FDA UDI | Class I | Active |
| SPII Model Lubinus | 128-984/35 | FDA UDI | Class II | Active |
| MP Monoblock Hip Stem | 136-117/46 | FDA UDI | Class II | Active |
| LINK Instrument | 165-810/30 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 317-585/95 | FDA UDI | Class I | Active |
| MobileLink Acetabular Cup System | 183-266/32 | FDA UDI | Class II | Unknown |
| Gemini SL | 318-237/10 | FDA UDI | Class II | Active |
| LINK Instruments - Saw and drill guides | 15-2201/58 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 151-005/03 | FDA UDI | Class I | Active |
| TrabecuLink Augments - Instruments | 185-210/10 | FDA UDI | Class I | Active |
| LinkSymphoKnee | 881-113/55 | FDA UDI | Class II | Active |
| LINK Endo-Model EVO Knee System | 15-4613/06 | FDA UDI | Class II | Active |
| SPII Model Lubinus | 127-748/26 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 881-115/30 | FDA UDI | Class II | Active |
| LINK Instrument | 183-162/04 | FDA UDI | Class I | Active |
| LINK Instruments - Saw and drill guides | 16-3241/00 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 151-712/20 | FDA UDI | Class I | Active |
| SPII Model Lubinus | 128-974/35 | FDA UDI | Class II | Active |
| MobileLink Acetabular Cup System - Instruments | 15-8380/01B | FDA UDI | Class I | Active |
| LINK Endo-Model EVO | 15-3950/27 | FDA UDI | Class II | Active |
| MobileLink Acetabular Cup System | 183-301/52 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-253/11 | FDA UDI | Class II | Active |
| LINK Endo-Model EVO Knee System | 15-3618/10 | FDA UDI | Class II | Active |
| Unicondylar Sled Prosthesis | 15-2028/06 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-299/16 | FDA UDI | Class II | Active |
| BiMobile | 184-270/01 | FDA UDI | Class II | Active |
| Prosthesis Head B | 198-836/02 | FDA UDI | Class II | Active |
| Endo-Model Modular Knee Prosthesis System | 15-2617/05 | FDA UDI | Class II | Active |
| LINK Instruments - Rasps, compressors and broaches | 130-555/04 | FDA UDI | Class I | Active |
| LINK Instruments - Trial implants and size gauges | 131-932/02 | FDA UDI | Class I | Active |
| LinkSymphoKnee | 880-311/11 | FDA UDI | Class II | Active |
| SPARK - Instruments | 445-602/10 | FDA UDI | Class I | Active |
| LinkSymphoKnee | 880-289/10 | FDA UDI | Class II | Active |
| LINK Instruments - Trial implants and size gauges | 99-0220/41 | FDA UDI | Class I | Active |
| Gemini SL | 318-248/16 | FDA UDI | Class II | Active |
| Gemini SL | 318-241/12 | FDA UDI | Class II | Active |
| LinkSymphoKnee | 880-325/23 | FDA UDI | Class II | Active |
| SPARK - Instruments | 445-405/14 | FDA UDI | Class I | Active |
| Endo-Model Knee System - Instruments | 75-3725 | FDA UDI | Class I | Active |
| LINK Instrument | 317-730/04 | FDA 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.