Utepreva, LLC
Country not established
- Devices
- 1
What Utepreva, LLC makes
Utepreva, LLC manufactures the Utepreva Endometrial Sampler (UP01), a device designed for obtaining endometrial tissue samples, primarily used in diagnostic procedures for conditions such as abnormal uterine bleeding or infertility.
The company’s product portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The device is based in the United States.
Catalogue
Utepreva Endometrial Sampler (UP01) Ref K240595
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Utepreva, LLC have in the registry?
The registry currently lists 1 device for Utepreva, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Utepreva, LLC's devices?
Among its 1 most recently registered device, Utepreva, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Utepreva, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Utepreva, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Utepreva, LLC in the registry?
The most recently registered devices listed for Utepreva, LLC include Utepreva Endometrial Sampler (UP01).