# Eurodent, Inc.

- Location (FDA's records): Canada  J4b 5z5, CA
- FDA decisions: 6 (1979–2005): 6 510(k) clearances
- Names in FDA's records: Eurodent, Inc. (5); Eurodent S.P.A. (1)
- Product codes: EIA (3), KLC (1), EAZ (1), ECG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K050571: Absolute America (Nov 2, 2005)
- K894058: Isodent (Dec 21, 1989)
- K894061: Studio Uno (Nov 21, 1989)
- K894060: Esse Quattro/Esse Uno (Sep 7, 1989)
- K894059: Isolight (Sep 7, 1989)
- K790078: Bar & Rider, Screws, Tubes (Feb 27, 1979)

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