# Dr. Fresh, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 2 (2012–2012): 2 510(k) clearances
- Product codes: EEG (1), LFD (1)
- Predicates its devices cite: 2 (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
- Dentovations, Inc.: 1 (https://510kreport.com/company/dentovations)
- Glaxosmithkline Consumer Healthcare (Gskch): 1 (https://510kreport.com/company/glaxosmithkline-consumer-healthcare-gskch)

## Firms that cite its devices most
- Dr. Harold Katz, LLC (Dba Therabreath: 1 (https://510kreport.com/company/dr-harold-katz-dba-therabreath)
- Syendgen, Inc.: 1 (https://510kreport.com/company/syendgen)

## Its most-cited devices
- K111250: Dry Mouth Mouthwash (2012), cited by 2

## Recent decisions
- K111250: Dry Mouth Mouthwash (Apr 27, 2012)
- K110888: Absolute White Light (Jan 12, 2012)

Source page: https://510kreport.com/company/dr-fresh