# Denplus, Inc.

- Location (FDA's records): Montreal, Quebec, CA
- FDA decisions: 2 (1999–2001): 2 510(k) clearances
- Product codes: EBI (2)
- 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
- K011762: HI-Wave; Pour-Plus (Aug 23, 2001)
- K991996: Impact-Plus, Impact-20, DP97, DP97-20, DP-Pour and DP-Repair (Sep 8, 1999)

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