# 3M Company Espe Dental Products

- Location (FDA's records): Saint Paul, MN
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: EBF (1)
- Predicates its devices cite: 2 (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
- 3M Company: 1 (https://510kreport.com/company/3m)
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)

## Firms that cite its devices most
- Guilin Kevin Peter Technology Co., Ltd.: 1 (https://510kreport.com/company/guilin-kevin-peter-technology)

## Its most-cited devices
- K221695: 3M Filtek Supreme Flowable Restorative (2022), cited by 1

## Recent decisions
- K221695: 3M Filtek Supreme Flowable Restorative (Jun 13, 2022)

Source page: https://510kreport.com/company/3m-company-espe-dental-products