# Mds

- Location (FDA's records): Great Neck, NY
- FDA decisions: 1 (2000–2000): 1 510(k) clearance
- Product codes: KIF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)

## Firms that cite its devices most
- Essential Dental Systems, Inc.: 1 (https://510kreport.com/company/essential-dental-systems)
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)

## Its most-cited devices
- K992727: The BI-Directional Spiral & Epoxy Root Canal Cement System (2000), cited by 2

## Recent decisions
- K992727: The BI-Directional Spiral & Epoxy Root Canal Cement System (Jan 18, 2000)

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