Oravanosa, LLC
Country not established
- Devices
- 1
What Oravanosa, LLC makes
Oravanosa, LLC manufactures the Oravan Herbst, a medical device classified as a Class II product.
The Oravan Herbst is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Oravan Herbst Ref K152159
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oravanosa, LLC have in the registry?
The registry currently lists 1 device for Oravanosa, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oravanosa, LLC's devices?
Among its 1 most recently registered device, Oravanosa, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Oravanosa, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oravanosa, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oravanosa, LLC in the registry?
The most recently registered devices listed for Oravanosa, LLC include Oravan Herbst.