Data / Medical devices / Bone Grafting Material, Synthetic / South Korea
FDA-registered makers of Bone Grafting Material, Synthetic in South Korea: 5 establishments
5 establishments in South Korea are registered with the FDA to make Bone Grafting Material, Synthetic (product code LYC). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Bone Grafting Material, Synthetic
- Product code
- LYC
- Country
- South Korea
Makers of Bone Grafting Material, Synthetic in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| GENOSS Co., Ltd. | Suwon-si Gyeonggi, South Korea | Manufacturer | 4 | September 14, 2016 | 0 | 0 | 0 | api.fda.gov |
| CG Bio Co., Ltd. | Hwaseong-si Gyeonggi, South Korea | Manufacturer | 1 | May 19, 2009 | 0 | 0 | 0 | api.fda.gov |
| Hudens Bio Co., Ltd. | Gwangju, South Korea | Manufacturer | 1 | March 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Meta Biomed Co., Ltd. | Cheongju-si Chungbuk, South Korea | Manufacturer | 1 | June 3, 2008 | 0 | 0 | 0 | api.fda.gov |
| Soyagreentec Co.,ltd | Hwaseong-si Gyeonggi, South Korea | Contract sterilizer, Manufacturer | 1 | April 24, 2007 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.