# Taeyeon Medical Co., Ltd.

- Location (FDA's records): Wonju-Si, KR
- FDA decisions: 3 (2007–2022): 3 510(k) clearances
- Product codes: MNI (1), NKB (1), HRX (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 4 (1 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
- D.K.M. Co., Ltd.: 1 (https://510kreport.com/company/dkm)
- U&I Corp., America: 1 (https://510kreport.com/company/u-i-america)
- Kyphon, Inc.: 1 (https://510kreport.com/company/kyphon)
- Imedicom Co., Ltd.: 1 (https://510kreport.com/company/imedicom)

## Firms that cite its devices most
- Norm Tibbi Urunler Ithalat Ihracat Sanayi VE Ticar: 1 (https://510kreport.com/company/norm-tibbi-urunler-ithalat-ihracat-sanayi-ve-ticar)
- OK Medinet Korea Co., Ltd.: 1 (https://510kreport.com/company/ok-medinet-korea)
- Mikron Makina Sanayi VE Ticaret Ltd. Sti.: 1 (https://510kreport.com/company/mikron-makina-sanayi-ve-ticaret-sti)

## Its most-cited devices
- K063708: 4S Spinal System (2007), cited by 3
- K202027: Balex bone Expander System (2021), cited by 1

## Recent decisions
- K212700: Dyflex-II (Nov 15, 2022)
- K202027: Balex bone Expander System (Feb 3, 2021)
- K063708: 4S Spinal System (Apr 24, 2007)

Source page: https://510kreport.com/company/taeyeon-medical