Stx-Med Sprl
BelgiumFDA applicant, unverified
- Devices
- 1
What Stx-Med Sprl makes
Stx-Med Sprl manufactures the CEFALY medical device, which is a Class II product.
The CEFALY device is regulated under the FDA 510(k) pathway and is listed in the fda_510k registry. Stx-Med Sprl is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cefaly Ref DEN120019
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Stx-Med Sprl have in the registry?
The registry currently lists 1 device for Stx-Med Sprl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stx-Med Sprl's devices?
Among its 1 most recently registered device, Stx-Med Sprl has devices listed in FDA 510(k) (1 device).
What risk classes do Stx-Med Sprl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stx-Med Sprl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stx-Med Sprl in the registry?
The most recently registered devices listed for Stx-Med Sprl include CEFALY.