# Seohancare Co., Ltd.

- Location (FDA's records): Gimpo-Si, KR
- FDA decisions: 1 (2020–2020): 1 510(k) clearance
- Product codes: NKB (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (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
- Medyssey USA, Inc.: 1 (https://510kreport.com/company/medyssey-usa)
- Dio Medical Co., Ltd.: 1 (https://510kreport.com/company/dio-medical)
- Bk Meditech, Co., Ltd.: 1 (https://510kreport.com/company/bk-meditech)
- Spinefrontier, Inc.: 1 (https://510kreport.com/company/spinefrontier)
- Pinnacle Spine Group, LLC: 1 (https://510kreport.com/company/pinnacle-spine-group)

## Recent decisions
- K191655: MEGAFIX® Pedicle Screw Spinal System (Mar 6, 2020)

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