Data / Medical devices / Cement, Dental / South Korea
FDA-registered makers of Cement, Dental in South Korea: 5 establishments
5 establishments in South Korea are registered with the FDA to make Cement, Dental (product code EMA). 5 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
- Cement, Dental
- Product code
- EMA
- Country
- South Korea
Makers of Cement, Dental 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 | 4 | June 20, 2025 | 0 | 0 | 0 | api.fda.gov |
| Diadent Group International | CHONGJU CITY Chungbuk, South Korea | Manufacturer | 1 | July 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Mediclus Co., Ltd | Cheongju-si Chungbuk, South Korea | Manufacturer | 1 | August 13, 2026 | 0 | 0 | 0 | api.fda.gov |
| Meta Biomed Co., Ltd. | Cheongju-si Chungbuk, South Korea | Manufacturer | 1 | May 15, 2018 | 0 | 0 | 0 | api.fda.gov |
| Vericom Co., Ltd. | Chuncheon-Si Gangwon, South Korea | Manufacturer | 1 | August 21, 2020 | 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.