Ipos KG
Country not established
- Devices
- 1
What Ipos KG makes
Ipos KG manufactures breast prostheses designed for post-mastectomy patients, providing form and volume restoration as part of reconstructive care.
The company’s breast prostheses are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Ipos Breast Prosthesis Ref K792372
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ipos KG have in the registry?
The registry currently lists 1 device for Ipos KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ipos KG's devices?
Among its 1 most recently registered device, Ipos KG has devices listed in FDA 510(k) (1 device).
What risk classes do Ipos KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ipos KG's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ipos KG in the registry?
The most recently registered devices listed for Ipos KG include IPOS BREAST PROSTHESIS.