Hortmann AG
Country not established
- Devices
- 2
What Hortmann AG makes
Hortmann AG manufactures Otoacoustic Emissions (OAE) analyzers, including the EchoMaster and AMDIS-OAE models, designed for assessing auditory function in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Hortmann Echomaster Oae Analyzer Ref K994033
Regimes: 510(k) Registry: 510(k)Hortmann Amdis-Oae Oae Analyzer Ref K980505
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hortmann AG have in the registry?
The registry currently lists 2 devices for Hortmann AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hortmann AG's devices?
Among its 2 most recently registered devices, Hortmann AG has devices listed in FDA 510(k) (2 devices).
What risk classes do Hortmann AG's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hortmann AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hortmann AG in the registry?
The most recently registered devices listed for Hortmann AG include HORTMANN ECHOMASTER OAE ANALYZER and HORTMANN AMDIS-OAE OAE ANALYZER.