# Espe Dental Products

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1977–1981): 8 510(k) clearances
- Product codes: EBF (2), EFD (1), EBZ (1), EBC (1), EMA (1), LEW (1), ELW (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- 3M Deutschland GmbH: 1 (https://510kreport.com/company/3m-deutschland)

## Its most-cited devices
- K800031: Permadyne Polyether Rubber Impression (1980), cited by 1

## Recent decisions
- K810950: Visio-Seal (Apr 29, 1981)
- K802819: Ketac-Cem in Ref. to K802048 (Nov 24, 1980)
- K802049: Nimetic-Dispers (Sep 16, 1980)
- K800031: Permadyne Polyether Rubber Impression (Feb 5, 1980)
- K771901: Capmix (Oct 20, 1977)
- K771889: Uniolite (Oct 20, 1977)
- K771120: Impreflex Alginate Impression Material (Aug 3, 1977)
- K771119: Pastes, Restorative & Tinted, Debtal (Jul 15, 1977)

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