Bebird Usa, Inc.
Country not established FDA establishment FEI 3035371880
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Bebird Usa, Inc. makes
Bebird USA, Inc. manufactures otoscopes and endoscopic devices, including the bebird model, designed for visual examination of ear canals and internal body structures.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identification (UDI) system. Bebird USA, Inc. is based in the United States.
Catalogue
- GUDID
Company details
- FDA FEI number
- 3035371880
- Address
- 2613 Manhattan Beach Blvd, Redondo Beach, CA, 90278
Frequently asked questions
How many devices does BEBIRD USA, INC. have in the registry?
The registry currently lists 1 device for BEBIRD USA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BEBIRD USA, INC.'s devices?
Among its 1 most recently registered device, BEBIRD USA, INC. has devices listed in FDA GUDID (1 device).
What risk classes do BEBIRD USA, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for BEBIRD USA, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from BEBIRD USA, INC. in the registry?
The most recently registered devices listed for BEBIRD USA, INC. include bebird W3-WM-BK.