Sohard AG
GermanyFDA applicant, unverified
- Devices
- 1
What Sohard AG makes
Sohard AG manufactures the RADIN, Model V 3.0, a Class II medical device designed for [specific function not provided in data]. This product is intended for [clinical use or application not detailed in data].
The RADIN, Model V 3.0 is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Radin, Model V 3.0 Ref K043483
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sohard AG have in the registry?
The registry currently lists 1 device for Sohard AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sohard AG's devices?
Among its 1 most recently registered device, Sohard AG has devices listed in FDA 510(k) (1 device).
What risk classes do Sohard AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sohard AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sohard AG in the registry?
The most recently registered devices listed for Sohard AG include RADIN, MODEL V 3.0.