Irradia AB
Country not established
- Devices
- 1
What Irradia AB makes
Irradia AB manufactures the IRRADIA MID, a laser device designed for medical applications. This system is intended for precise tissue treatment, likely within dermatological or ophthalmological procedures.
The IRRADIA MID laser is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Irradia Mid - Laser (S3) Ref K051548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Irradia AB have in the registry?
The registry currently lists 1 device for Irradia AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Irradia AB's devices?
Among its 1 most recently registered device, Irradia AB has devices listed in FDA 510(k) (1 device).
What risk classes do Irradia AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Irradia AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Irradia AB in the registry?
The most recently registered devices listed for Irradia AB include IRRADIA MID - LASER (S3).