# Cynovad

- Location (FDA's records): St Laurent, Quebec, CA
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: EIH (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 6 (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
- Dentronic AB: 1 (https://510kreport.com/company/dentronic)
- Degussa - Ney Dental, Inc.: 1 (https://510kreport.com/company/degussa-ney-dental)
- Vident: 1 (https://510kreport.com/company/vident)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)

## Firms that cite its devices most
- Acucera, Inc.: 1 (https://510kreport.com/company/acucera)
- Charles Scharf: 1 (https://510kreport.com/company/charles-scharf)
- Sagemax Bioceramics, Inc.: 1 (https://510kreport.com/company/sagemax-bioceramics)
- Medin Tech: 1 (https://510kreport.com/company/medin-tech)
- P.S.L. International, Inc.: 1 (https://510kreport.com/company/psl-international)
- Cerasys, Inc.: 1 (https://510kreport.com/company/cerasys)

## Its most-cited devices
- K023327: Cynovad Zirkon (2002), cited by 6

## Recent decisions
- K023327: Cynovad Zirkon (Dec 2, 2002)

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