Dentkist, Inc.
South KoreaFDA applicant, unverified FDA FEI 3013012934
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Company details
- FDA FEI number
- 3013012934
- Address
- (Dangjeong-dong) 3, Nongshim-ro, Gunpo-si Gyeonggi
Frequently asked questions
How many devices does Dentkist, Inc. have in the registry?
The registry currently lists 2 devices for Dentkist, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentkist, Inc.'s devices?
Among its 2 most recently registered devices, Dentkist, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dentkist, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dentkist, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dentkist, Inc. in the registry?
The most recently registered devices listed for Dentkist, Inc. include CharmFlex and CharmFil.