# Dms Co., Ltd.

- Location (FDA's records): Wonju-Si, KR
- FDA decisions: 2 (1993–2019): 2 510(k) clearances
- Names in FDA's records: Dms Co., Ltd. (1); Dms (1)
- Product codes: EKX (1), FPP (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Osstell AB: 1 (https://510kreport.com/company/osstell)

## Firms that cite its devices most
- Genoss Co., Ltd.: 1 (https://510kreport.com/company/genoss)

## Its most-cited devices
- K180953: AnyCheck IMT-100 (2019), cited by 1

## Recent decisions
- K180953: AnyCheck IMT-100 (Feb 20, 2019)
- K924275: Restraining Stretcher (Jul 27, 1993)

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