Mentice Spain S.L.
SpainFDA applicant, unverified FDA FEI 3038611208
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Company details
- FDA FEI number
- 3038611208
- DUNS number
- 471570274
- Address
- Rambla Catalunya, 53-55, Barcelona Catalonia
Frequently asked questions
How many devices does Mentice Spain S.L. have in the registry?
The registry currently lists 3 devices for Mentice Spain S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mentice Spain S.L.'s devices?
Among its 3 most recently registered devices, Mentice Spain S.L. has devices listed in EUDAMED (1 device), FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Mentice Spain S.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mentice Spain S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mentice Spain S.L. in the registry?
The most recently registered devices listed for Mentice Spain S.L. include ANKYRAS v4.0.4-US and Ankyras.