Id Lightcure System Id Crown Kit
Listed
Valid until
Not applicable
FDA recalls
None foundDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08809896991049 | Date14 May 2026 | StatusListed |
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Id Lightcure System
- Generic Name
- Dental unfilled resin sealant/coating
- Model / Reference
- ID CROWN KIT
- Primary DI / UDI-DI
- 08809896991049
- 510(k) Number
- FDA Product Code
- EBD
- GMDN Term
- Dental unfilled resin sealant/coating
- Device Class
- Class II
- Regulation Number
- 872.3310
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 54 Gram
Other devices from Id Korea Co., Ltd.
Properties
Other properties (8)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No