Mojca Valijavec
SloveniaFDA applicant, unverified
- Devices
- 1
What Mojca Valijavec makes
Mojca Valijavec manufactures ND:YAG laser systems, including the FOTONA DUALIS and FOTONA TWINLIGHT models, designed for medical laser treatments.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mojca Valijavec have in the registry?
The registry currently lists 1 device for Mojca Valijavec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mojca Valijavec's devices?
Among its 1 most recently registered device, Mojca Valijavec has devices listed in FDA 510(k) (1 device).
What risk classes do Mojca Valijavec's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mojca Valijavec's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mojca Valijavec in the registry?
The most recently registered devices listed for Mojca Valijavec include FOTONA DUALIS ND:YAG LASER SYSTEM, FOTONA TWINLIGHT ND:YAG LASER SYSTEM.