Id Korea Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3039359767
- Devices
- 64
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Id Korea Co., Ltd. makes
Id Korea Co., Ltd. manufactures the ID Light Cure System, a device designed for curing dental composites and adhesives using light activation technology.
The ID Light Cure System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 64 devicesShowing 1-50 of 64
Company details
- FDA FEI number
- 3039359767
- DUNS number
- 694785677
- Address
- 405, 150, Donggyecheon-ro, Dong-gu Gwangju
- [email protected]
- Phone
- +8207047793000
Frequently asked questions
How many devices does Id Korea Co., Ltd. have in the registry?
The registry currently lists 64 devices for Id Korea Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Id Korea Co., Ltd.'s devices?
Among its 50 most recently registered devices, Id Korea Co., Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Id Korea Co., Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Id Korea Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Id Korea Co., Ltd. in the registry?
The most recently registered devices listed for Id Korea Co., Ltd. include ID LIGHTCURE SYSTEM GUM FLOW PINK, ID LIGHTCURE SYSTEM GUM FLOW GRANATE, ID LIGHTCURE SYSTEM GUM FLOW LIGHT PINK and ID LIGHTCURE SYSTEM GUM FLOW PEACH.