Sanpoint AB
SwedenFDA applicant, unverified
- Devices
- 1
What Sanpoint AB makes
Sanpoint AB manufactures menstrual tampons designed for internal use during menstruation. These products are intended for single-use absorption of menstrual flow and are constructed with materials suitable for vaginal insertion.
The company’s menstrual tampon is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The product is regulated under US jurisdiction, where Sanpoint AB is based.
Catalogue
Sanpoint Menstrual Tampon Ref K961926
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanpoint AB have in the registry?
The registry currently lists 1 device for Sanpoint AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanpoint AB's devices?
Among its 1 most recently registered device, Sanpoint AB has devices listed in FDA 510(k) (1 device).
What risk classes do Sanpoint AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sanpoint AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanpoint AB in the registry?
The most recently registered devices listed for Sanpoint AB include SANPOINT MENSTRUAL TAMPON.