# D.K.M. Co., Ltd.

- Location (FDA's records): St. Louis, MO
- FDA decisions: 1 (2000–2000): 1 510(k) clearance
- Product codes: MNH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 16 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Advanced Spine Technology, Inc.: 1 (https://510kreport.com/company/advanced-spine-technology)

## Firms that cite its devices most
- Solco Biomedical Co., Ltd.: 5 (https://510kreport.com/company/solco-biomedical)
- L&K BIOMED Co., Ltd.: 2 (https://510kreport.com/company/l-k-biomed)
- U&I Corporation: 2 (https://510kreport.com/company/u-i)
- GS Medical Co., Ltd.: 1 (https://510kreport.com/company/gs-medical)
- Taeyeon Medical Co., Ltd.: 1 (https://510kreport.com/company/taeyeon-medical)
- Alphatec Mfg., Inc.: 1 (https://510kreport.com/company/alphatec-mfg)
- Implanova Co., Ltd.: 1 (https://510kreport.com/company/implanova)
- Signus Medical, LLC: 1 (https://510kreport.com/company/signus-medical)

## Its most-cited devices
- K001668: Global Spinal Fixation System (2000), cited by 16

## Recent decisions
- K001668: Global Spinal Fixation System (Oct 19, 2000)

Source page: https://510kreport.com/company/dkm