Data / Medical devices / Material, Tooth Shade, Resin / South Korea
FDA-registered makers of Material, Tooth Shade, Resin in South Korea: 12 establishments
12 establishments in South Korea are registered with the FDA to make Material, Tooth Shade, Resin (product code EBF). 9 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Material, Tooth Shade, Resin
- Product code
- EBF
- Country
- South Korea
Makers of Material, Tooth Shade, Resin in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Spident Co., Ltd. | INCHEON Gyeonggi, South Korea | Manufacturer | 6 | May 30, 2025 | 0 | 0 | 0 | api.fda.gov |
| Vericom Co., Ltd. | Chuncheon-Si Gangwon, South Korea | Manufacturer | 6 | May 11, 2026 | 0 | 0 | 0 | api.fda.gov |
| Diadent Group International | CHONGJU CITY Chungbuk, South Korea | Manufacturer | 5 | June 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Mediclus Co., Ltd | Cheongju-si Chungbuk, South Korea | Manufacturer | 5 | December 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Meta Biomed Co., Ltd. | Cheongju-si Chungbuk, South Korea | Manufacturer | 4 | October 8, 2024 | 0 | 0 | 0 | api.fda.gov |
| GENOSS Co., Ltd. | Suwon-si Gyeonggi, South Korea | Manufacturer | 2 | November 30, 2020 | 0 | 0 | 0 | api.fda.gov |
| Graphy Inc. | Seoul, South Korea | Exporter to the US, Manufacturer | 2 | November 1, 2023 | 0 | 0 | 0 | api.fda.gov |
| ARUM DENTISTRY Co., Ltd. | Yuseong-gu Daejeon, South Korea | Manufacturer | 1 | September 11, 2024 | 0 | 0 | 0 | api.fda.gov |
| Hdi Inc. | Seongnam-si Gyeonggi, South Korea | Manufacturer | 1 | September 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Dentkist, Inc. | Gunpo-si Gyeonggi, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Id Korea Co., Ltd. | Dong-gu Gwangju, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SMD Dental Laboratory | Heungdeok-gu Cheongju-si Chungbuk, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.