Manufacturer registered with FDA
Id Korea Co., Ltd.
Dong-gu, South Korea. Lists 4 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 12025–2025
- Markets registered in
- 1United States
- Establishments
- 1South Korea
510(k) clearances per year, 2007–2026
Devices listed with FDA
What Id Korea Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Resin Filling Material CoatingEBD · Class 2 | — | Maker | ID Light Cure System | 2025 |
| Resin Tooth Shade MaterialEBF · Class 2 | Dental composites | Maker | ID Light Cure System | 2025 |
| Rebasing Repairing Relining Denture ResinEBI · Class 2 | Denture resins & teeth | Maker | ID Light Cure System | 2025 |
| Preformed Tooth PositionerKMY · Class 1 | Retainers, expanders & headgear | Maker | ID Light Cure System | 2025 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| ID KOREA CO., LTD.FDA reg. 3039359767 | Dong-gu Gwangju, South Korea | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10093594). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.