Reoss GmbH
GermanyFDA applicant, unverified FDA FEI 3017734069
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Reoss GmbH makes
Reoss GmbH makes dental and maxillofacial surgical mesh devices, including products such as Yxoss and Yxoss CBR®.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries; the company is based in the United States.
Catalogue
- Registry: GUDID
Yxoss CBR® Ref K192747
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017734069
- DUNS number
- 341422829
- Address
- Echterdinger Str. 57, Filderstadt Baden-Wurttemberg
Frequently asked questions
How many devices does Reoss GmbH have in the registry?
The registry currently lists 2 devices for Reoss GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reoss GmbH's devices?
Among its 2 most recently registered devices, Reoss GmbH has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Reoss GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Reoss GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reoss GmbH in the registry?
The most recently registered devices listed for Reoss GmbH include Yxoss CBR and Yxoss CBR®.