Solius Labs, Inc.
United Statesfrom the FDA registration address FDA FEI 3018702411
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Solius Labs, Inc. makes
Solius Labs, Inc. manufactures the SOLIUS PRO UVB Light Panel, a medical device designed for therapeutic ultraviolet B (UVB) light exposure, primarily used in dermatological treatments.
The SOLIUS PRO UVB Light Panel is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
SOLIUS PRO UVB Light Panel Ref K252960
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3018702411
- DUNS number
- 037916336
- Address
- 100 Ravine Lane NE, Bainbridge Island, WA, 98110
Frequently asked questions
How many devices does Solius Labs, Inc. have in the registry?
The registry currently lists 9 devices for Solius Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solius Labs, Inc.'s devices?
Among its 9 most recently registered devices, Solius Labs, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Solius Labs, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Solius Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solius Labs, Inc. in the registry?
The most recently registered devices listed for Solius Labs, Inc. include Solius Solius Pro, Solius Solius iOS App, Solius Solius Android App and Solius Solius Protective Eyewear.