Augmented Reality Software S.L.
SpainFDA 510(k) applicant, unverified
- Devices
- 1
What Augmented Reality Software S.L. makes
Augmented Reality Software S.L. develops the LAIA XR, an augmented reality software platform designed for medical training and procedural guidance, integrating real-time visual overlays with patient data for enhanced clinical decision-making.
The LAIA XR system is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Laia Xr Ref K251577
CE MDR 510(k) 510(k)
Frequently asked questions
How many devices does Augmented Reality Software S.L. have in the registry?
The registry currently lists 1 device for Augmented Reality Software S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Augmented Reality Software S.L.'s devices?
Among its 1 most recently registered device, Augmented Reality Software S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Augmented Reality Software S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Augmented Reality Software S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Augmented Reality Software S.L. in the registry?
The most recently registered devices listed for Augmented Reality Software S.L. include LAIA XR.