Benilight
Country not established
Benilight is a medical device manufacturer, with 4 devices listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 4
Registry facts
- Registries
- FDA GUDID 4
- Device classes
- FDA Class II 4
- Sites and related companies
- Benilight South Korea
- Identifiers
- DUNS 695132580
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 695132580
- slim@benilight.com
- Phone
- +821037229599
Sites
- Benilight KRFEI 3024838204 0 devices
Frequently asked questions
How many devices does Benilight have in the registry?
The registry currently lists 4 devices for Benilight. Devices recorded under merged duplicate company entries are counted once.
Which registries list Benilight's devices?
Among its 4 most recently registered devices, Benilight has devices listed in FDA GUDID (4 devices).
What risk classes do Benilight's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Benilight's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Benilight in the registry?
The most recently registered devices listed for Benilight include Benilight iLED-Pro Mini, Benilight iLED-Pro, Benilight Life Beam and Benilight iLED.