Brazen Goods Inc. Dba Lorals
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- Devices
- 1
What Brazen Goods Inc. Dba Lorals makes
Brazen Goods Inc. dba Lorals manufactures the Lorals device, a Class II medical product designed for use in the female pelvic health space, specifically for vaginal support and prolapse treatment.
The Lorals device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Lorals Ref K212928
510(k) 510(k)
Frequently asked questions
How many devices does Brazen Goods Inc. Dba Lorals have in the registry?
The registry currently lists 1 device for Brazen Goods Inc. Dba Lorals. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brazen Goods Inc. Dba Lorals's devices?
Among its 1 most recently registered device, Brazen Goods Inc. Dba Lorals has devices listed in FDA 510(k) (1 device).
What risk classes do Brazen Goods Inc. Dba Lorals's devices fall under?
Among its 1 most recently registered device, the classes recorded for Brazen Goods Inc. Dba Lorals's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brazen Goods Inc. Dba Lorals in the registry?
The most recently registered devices listed for Brazen Goods Inc. Dba Lorals include Lorals.