Neomedic International S.L.
Also registered as Neomedic International
Country not established FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
Surelift Prolapse System Ref K102815
510(k) 510(k)Kim Ref K103022
510(k) 510(k)Anchorsure Ref K120831
510(k) 510(k)
FDA establishments
- Neomedic International TERRASA Barcelona · ES FEI 3004838863
Frequently asked questions
How many devices does Neomedic International S.L. have in the registry?
The registry currently lists 3 devices for Neomedic International S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neomedic International S.L.'s devices?
Among its 3 most recently registered devices, Neomedic International S.L. has devices listed in FDA 510(k) (3 devices).
What risk classes do Neomedic International S.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neomedic International S.L.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Neomedic International S.L. in the registry?
The most recently registered devices listed for Neomedic International S.L. include SURELIFT PROLAPSE SYSTEM, KIM and ANCHORSURE.
Which FDA establishments are linked to Neomedic International S.L.?
1 FDA establishment is linked to Neomedic International S.L. in the registry; they are listed on the company page.