# Yeti Dentalprodukte GmbH

- Location (FDA's records): Engen, DE
- FDA decisions: 1 (2018–2018): 1 510(k) clearance
- Product codes: EIH (1)
- Predicates its devices cite: 3 (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

## Firms whose devices it cites most
- Metoxit AG: 1 (https://510kreport.com/company/metoxit)
- Amann Girrbach America, Inc.: 1 (https://510kreport.com/company/amann-girrbach-america)
- Emergo Europe Consulting BV: 1 (https://510kreport.com/company/emergo-europe-consulting)

## Recent decisions
- K173971: K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent (Nov 15, 2018)

Source page: https://510kreport.com/company/yeti-dentalprodukte