Alm S.A.
Country not established
- Devices
- 2
What Alm S.A. makes
Alm S.A. manufactures surgical light systems, including the ALM X'TEN (X10) surgical light system and modifications to the Prismalix surgical light.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Modification To Prismalix Surgical Light Ref K040015
Regimes: 510(k) Registry: 510(k)Alm X'ten (X10) Surgical Light System Ref K040735
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alm S.A. have in the registry?
The registry currently lists 2 devices for Alm S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alm S.A.'s devices?
Among its 2 most recently registered devices, Alm S.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alm S.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alm S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alm S.A. in the registry?
The most recently registered devices listed for Alm S.A. include MODIFICATION TO PRISMALIX SURGICAL LIGHT and ALM X'TEN (X10) SURGICAL LIGHT SYSTEM.