Ansella Therapeutics
Country not established
- Devices
- 1
What Ansella Therapeutics makes
Ansella Therapeutics manufactures the Cerynë Intimate Care product line, which includes medical-grade incontinence pads and protective undergarments designed for adult pelvic health management.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. Ansella Therapeutics is based in the United States.
Catalogue
Cerynë Intimate Care Ref K250488
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ansella Therapeutics have in the registry?
The registry currently lists 1 device for Ansella Therapeutics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ansella Therapeutics's devices?
Among its 1 most recently registered device, Ansella Therapeutics has devices listed in FDA 510(k) (1 device).
What risk classes do Ansella Therapeutics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ansella Therapeutics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ansella Therapeutics in the registry?
The most recently registered devices listed for Ansella Therapeutics include Cerynë Intimate Care.