Artimplant AB
Country not established
- Devices
- 7
What Artimplant AB makes
Artimplant AB manufactures medical devices for orthopedic and soft tissue reinforcement, including cementless spacers for joint arthroplasty (e.g., ARTELON SPACER CMC-1, ARTELON STT SPACER) and tissue reinforcement meshes (e.g., SPORTMESH). Their portfolio also includes absorbable and non-absorbable surgical sutures designed for orthopedic and soft tissue applications.
The company’s devices are classified under FDA Class II and are listed via 510(k) clearance. These products are intended for use in the United States, where regulatory compliance is maintained through the FDA’s premarket notification process.
Catalogue
Artelon Spacer Cmc-1 Ref K040070
Regimes: 510(k) Registry: 510(k)Artelon Cmc Spacer Arthro Ref K061954
Regimes: 510(k) Registry: 510(k)Sportmesh Or Artelon Tissue Reinforcement Ref K071887
Regimes: 510(k) Registry: 510(k)Artelon Stt Spacer Ref K061956
Regimes: 510(k) Registry: 510(k)Artelon Surgical Suture Ref K052482
Regimes: 510(k) Registry: 510(k)Sportmesh Ref K052830
Regimes: 510(k) Registry: 510(k)Artelon Surgical Suture Ref K032160
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artimplant AB have in the registry?
The registry currently lists 7 devices for Artimplant AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artimplant AB's devices?
Among its 7 most recently registered devices, Artimplant AB has devices listed in FDA 510(k) (7 devices).
What risk classes do Artimplant AB's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Artimplant AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artimplant AB in the registry?
The most recently registered devices listed for Artimplant AB include ARTELON SPACER CMC-1, ARTELON CMC SPACER ARTHRO, SPORTMESH OR ARTELON TISSUE REINFORCEMENT and ARTELON STT SPACER.