# Bredent GmbH & Co. KG

- Location (FDA's records): Senden, DE
- FDA decisions: 3 (2010–2024): 3 510(k) clearances
- Product codes: EBF (1), EBD (1), ELM (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (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
- Bicon, Inc.: 1 (https://510kreport.com/company/bicon)
- Juvora: 1 (https://510kreport.com/company/juvora)
- GC America, Inc.: 1 (https://510kreport.com/company/gc-america)
- Ivoclar North America, Inc.: 1 (https://510kreport.com/company/ivoclar-north-america)

## Firms that cite its devices most
- Merz Dental GmbH: 1 (https://510kreport.com/company/merz-dental)
- Cendres & Metaux SA: 1 (https://510kreport.com/company/cendres-metaux)
- Zirkonzahn Srl: 1 (https://510kreport.com/company/zirkonzahn)

## Its most-cited devices
- K152113: BioHPP - breCAM.BioHPP (2016), cited by 3

## Recent decisions
- K240735: visio.lign color, visio.lign shield (Dec 12, 2024)
- K152113: BioHPP - breCAM.BioHPP (Jul 21, 2016)
- K101064: Bredent Novo.Lign a/ Bredent Novo.Lign P (Sep 14, 2010)

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