Data / Medical devices / South Korea / Id Korea Co., Ltd.
Id Korea Co., Ltd.: FDA-registered device maker in Dong-gu Gwangju, South Korea, 1 510(k) clearance
Id Korea Co., Ltd. is registered with the FDA (registration 3039359767) in Dong-gu Gwangju, South Korea. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 4, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039359767
- Address
- 405, 150, Donggyecheon-ro, Dong-gu Gwangju, South Korea, 61436
- Owner or operator
- ID KOREA CO., LTD. (10093594)
- Roles
- Manufacturer
- First device listed
- June 10, 2025
- Registered through
- 2026
- Brand names listed
- ID Light Cure System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Coating, Filling Material, Resin | EBD | 2 | Manufacturer | accessdata.fda.gov |
| Material, Tooth Shade, Resin | EBF | 2 | Manufacturer | accessdata.fda.gov |
| Mouthguard, Prescription | MQC | U | Manufacturer | accessdata.fda.gov |
| Positioner, Tooth, Preformed | KMY | 1 | Manufacturer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 4, 2025 | K250804 | ID LIGHT CURE SYSTEM | EBD | Substantially Equivalent | Id Korea Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mouthguard, Prescription
- All makers of Material, Tooth Shade, Resin
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Coating, Filling Material, Resin
- All makers of Positioner, Tooth, Preformed
Updated June 4, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.