Dreamgard, Inc.
Country not established
- Devices
- 1
What Dreamgard, Inc. makes
Dreamgard, Inc. manufactures a range of Class II, non-invasive respiratory devices designed for sleep apnea management, including the DREAMGARD REM-SOFT, REM-LITE, REM-ULTRA, and REM-MAX. These products are intended for use as oral appliances to treat obstructive sleep apnea by repositioning the jaw and airway during sleep.
The company’s devices are regulated under the U.S. Food and Drug Administration’s 510(k) pathway and are listed in the FDA’s 510(k) database. The portfolio is classified under Class II medical devices and is intended for commercial distribution within the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Dreamgard, Inc. have in the registry?
The registry currently lists 1 device for Dreamgard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dreamgard, Inc.'s devices?
Among its 1 most recently registered device, Dreamgard, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Dreamgard, Inc. in the registry?
The most recently registered devices listed for Dreamgard, Inc. include DREAMGARD REM-SOFT, DREAMGARD REM-LITE, DREAMGARD REM-ULTRA, DREAMGARD REM-MAX.