# D&S Redhage

- Location (FDA's records): New Haven, MO
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: LRK (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
- Snore - Ezzer: 1 (https://510kreport.com/company/snore-ezzer)
- Marketing Technologies, Inc.: 1 (https://510kreport.com/company/marketing-technologies)
- Nellcor Puritan Bennett, Inc.: 1 (https://510kreport.com/company/nellcor-puritan-bennett)
- W. Keith Thornton, D.D.S.: 1 (https://510kreport.com/company/w-keith-thornton-dds)

## Firms that cite its devices most
- Bryan Keropian Dds: 2 (https://510kreport.com/company/bryan-keropian-dds)
- Mark Abramson, D.D.S., Inc.: 1 (https://510kreport.com/company/mark-abramson-dds)

## Its most-cited devices
- K022891: The Breathe EZ Anti-Snoring Device (2003), cited by 3

## Recent decisions
- K022891: The Breathe EZ Anti-Snoring Device (Feb 19, 2003)

Source page: https://510kreport.com/company/d-s-redhage