# Dreamgard, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: MQC (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Mci-Myohealth Systems: 1 (https://510kreport.com/company/mci-myohealth-systems)

## Recent decisions
- K112868: Dreamgard Rem-Soft, Dreamgard Rem-Lite, Dreamgard Rem-Ultra, Dreamgard Rem-Max (Jan 19, 2012)

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