Laon Medi, Inc.
South KoreaFDA applicant, unverified FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Laon Medi, Inc. makes
Laon Medi, Inc. makes Align Studio, Laon Ortho
Laon Medi, Inc. is based in the US and its devices are listed in the FDA 510(k) registry as Class II medical devices.
Catalogue
- Registry: GUDID
Align Studio Ref K232564
Regimes: 510(k) Registry: 510(k)Laon Ortho Ref K250198
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 695282782
- [email protected]
- Phone
- +82025078990
FDA establishments
- Laon Medi Inc. Gwacheon-si, Gyeonggi-do · KR FEI 3042204491
Frequently asked questions
How many devices does Laon Medi, Inc. have in the registry?
The registry currently lists 3 devices for Laon Medi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laon Medi, Inc.'s devices?
Among its 3 most recently registered devices, Laon Medi, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Laon Medi, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Laon Medi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laon Medi, Inc. in the registry?
The most recently registered devices listed for Laon Medi, Inc. include Laon Ortho 2.0, Align Studio and Laon Ortho.
Which FDA establishments are linked to Laon Medi, Inc.?
1 FDA establishment is linked to Laon Medi, Inc. in the registry; they are listed on the company page.