Pontemedag
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Pontemedag makes
Pontemedag manufactures the PELVIPOWER Pelvic Functional Magnetic Stimulation (PelvicFMS), a device designed for pelvic floor stimulation therapy. This system is intended to address pelvic floor dysfunction through non-invasive magnetic stimulation.
The PELVIPOWER PelvicFMS is classified as a Class II medical device in the United States and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02) Ref K252334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pontemedag have in the registry?
The registry currently lists 1 device for Pontemedag. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pontemedag's devices?
Among its 1 most recently registered device, Pontemedag has devices listed in FDA 510(k) (1 device).
What risk classes do Pontemedag's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pontemedag's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pontemedag in the registry?
The most recently registered devices listed for Pontemedag include PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02).