# Vivadent (Usa), Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 17 (1978–1986): 17 510(k) clearances
- Product codes: EBF (4), EMA (3), EBC (2), EBD (1), DYH (1), EJK (1), EAY (1), EBG (1), EJJ (1), EBL (1), KLE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bredent-Products For the Dental Technician Laborat: 1 (https://510kreport.com/company/bredent-products-for-the-dental-technician-laborat)
- Gebdi Dental-Products GmbH: 1 (https://510kreport.com/company/gebdi-dental-products)

## Its most-cited devices
- K790439: Contact Resin (1979), cited by 2

## Recent decisions
- K863831: Vivadent Filpin (Oct 14, 1986)
- K823409: Heliosit-Orthodontic (Jan 21, 1983)
- K813015: Helioseal (Dec 2, 1981)
- K802679: Silanit (Dec 17, 1980)
- K802684: Heliomat (Nov 24, 1980)
- K802683: Heliosit (Nov 24, 1980)
- K802682: Contact Seal (Nov 24, 1980)
- K802681: Heliobond (Nov 24, 1980)

Source page: https://510kreport.com/company/vivadent-usa