Friedrichsfeld Medizintechnik AG
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- Devices
- 1
What Friedrichsfeld Medizintechnik AG makes
Friedrichsfeld Medizintechnik AG manufactures the CERAVITAL Middle Ear Implant, a device designed for auditory restoration in patients with specific conductive or mixed hearing losses. This implant is intended to mechanically transmit sound from the middle ear to the inner ear, improving hearing function without requiring external amplification.
The CERAVITAL Middle Ear Implant is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Ceravital Middle Ear Implant Ref K913619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Friedrichsfeld Medizintechnik AG have in the registry?
The registry currently lists 1 device for Friedrichsfeld Medizintechnik AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Friedrichsfeld Medizintechnik AG's devices?
Among its 1 most recently registered device, Friedrichsfeld Medizintechnik AG has devices listed in FDA 510(k) (1 device).
What risk classes do Friedrichsfeld Medizintechnik AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Friedrichsfeld Medizintechnik AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Friedrichsfeld Medizintechnik AG in the registry?
The most recently registered devices listed for Friedrichsfeld Medizintechnik AG include CERAVITAL MIDDLE EAR IMPLANT.