# Remedent NV

- Location (FDA's records): Claremont, NH
- FDA decisions: 2 (2003–2009): 2 510(k) clearances
- Product codes: LBH (1), EBZ (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Ultradent Products, Inc.: 1 (https://510kreport.com/company/ultradent-products)
- Del Pharmaceuticals, Inc.: 1 (https://510kreport.com/company/del-pharmaceuticals)
- Phoenix Dental, Inc.: 1 (https://510kreport.com/company/phoenix-dental)
- Coll Partners, Ltd.: 1 (https://510kreport.com/company/coll-partners)

## Firms that cite its devices most
- Centrix, Inc.: 1 (https://510kreport.com/company/centrix)
- Sylphar N.V.: 1 (https://510kreport.com/company/sylphar)

## Its most-cited devices
- K082594: Remesense (2009), cited by 2

## Recent decisions
- K082594: Remesense (Mar 19, 2009)
- K023652: Remecure Model CL 15E (Jan 9, 2003)

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