Loon Lab Inc.
Country not established
Loon Lab Inc. is a medical device manufacturer, with 8 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 8
Registry facts
- Registries
- FDA GUDID 8
- Device classes
- FDA Class II 8
- Identifiers
- DUNS 694613996
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 694613996
- cs@leonacup.com
- Phone
- +827041646699
Frequently asked questions
How many devices does LOON LAB INC. have in the registry?
The registry currently lists 8 devices for LOON LAB INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LOON LAB INC.'s devices?
Among its 8 most recently registered devices, LOON LAB INC. has devices listed in FDA GUDID (8 devices).
What risk classes do LOON LAB INC.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for LOON LAB INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LOON LAB INC. in the registry?
The most recently registered devices listed for LOON LAB INC. include LEONA BASIC SMALL, LEONA AIR FLOW SMALL, LEONA AIR FLOW LARGE and LEONA BASIC LARGE.