Argomedical AG
Country not established
- Devices
- 1
What Argomedical AG makes
Argomedical AG manufactures the EPOCA Custom Offset Shoulder System, a medical device designed for orthopedic applications to address shoulder joint alignment and mobility issues. This system is intended for surgical use in procedures requiring precise anatomical adjustments, such as reverse shoulder arthroplasty or other corrective surgeries.
The EPOCA Custom Offset Shoulder System is classified as a Class II device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States, and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Epoca Custom Offset Shoulder System Ref K010869
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Argomedical AG have in the registry?
The registry currently lists 1 device for Argomedical AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argomedical AG's devices?
Among its 1 most recently registered device, Argomedical AG has devices listed in FDA 510(k) (1 device).
What risk classes do Argomedical AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Argomedical AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argomedical AG in the registry?
The most recently registered devices listed for Argomedical AG include EPOCA CUSTOM OFFSET SHOULDER SYSTEM.