Rosesta Medical BV
NetherlandsFDA applicant, unverified
- Devices
- 1
What Rosesta Medical BV makes
Rosesta Medical BV manufactures the FERTI-LILY Conception Cup, a device designed for fertility tracking and ovulation detection, intended for use by women to identify their fertile window.
The FERTI-LILY Conception Cup is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
FERTI-LILY Conception Cup Ref K222969
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rosesta Medical BV have in the registry?
The registry currently lists 1 device for Rosesta Medical BV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rosesta Medical BV's devices?
Among its 1 most recently registered device, Rosesta Medical BV has devices listed in FDA 510(k) (1 device).
What risk classes do Rosesta Medical BV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rosesta Medical BV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rosesta Medical BV in the registry?
The most recently registered devices listed for Rosesta Medical BV include FERTI-LILY Conception Cup.