Bleep, LLC
United Statesfrom the FDA registration address FDA FEI 3015436853
Bleep, LLC is a medical device manufacturer, with 23 devices listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 23
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 23
- Device classes
- FDA Class II 23
- Identifiers
- FDA FEI 3015436853
- DUNS 081909526
At a glance
Market reach
- United States
- FDA FEI
What Bleep, LLC makes
BLEEP, LLC manufactures home CPAP units and related accessories, including vent filters, vent diffusers, connector kits, tube management systems, and magnetic port replacement packs. Specific products include the Bleep Dreamway, Eclipse Vent Filter and Diffuser Kits, Dreamprep, and Dreamway clinical and connector kits.
The devices are classified as Class II medical devices and are listed in the FDA’s Unique Device Identification (FDA UDI) system.
Catalogue
Search and filter all 23 devicesCompany details
- FDA FEI number
- 3015436853
- DUNS number
- 081909526
- Address
- 11312 US 15-501 North, Chapel Hill, NC, 27517
- info@bleepeep.com
- Phone
- 1-833-392-5337
Frequently asked questions
How many devices does BLEEP, LLC have in the registry?
The registry currently lists 23 devices for BLEEP, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list BLEEP, LLC's devices?
Among its 23 most recently registered devices, BLEEP, LLC has devices listed in FDA GUDID (23 devices).
What risk classes do BLEEP, LLC's devices fall under?
Among its 23 most recently registered devices, the classes recorded for BLEEP, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BLEEP, LLC in the registry?
The most recently registered devices listed for BLEEP, LLC include Vent filter 24 pack 100595, Vent diffuser kit - Quarterly supply 100593, Bleep Dreamway 100380 and Eclipse Vent Filter Replacement Pack 100662.