Be Technologies, Inc.
Country not established
Be Technologies, Inc. is a medical device manufacturer, with 1 device listed in FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 1
Registry facts
- Registries
- FDA 510(k) 1
- Device classes
- FDA Class II 1
What Be Technologies, Inc. makes
Be Technologies, Inc. manufactures uroflowmeters, which are diagnostic devices used to measure the flow rate and volume of urine during voiding. These instruments help assess urinary function and detect potential lower urinary tract issues.
The company’s uroflowmeters are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance pathway. The devices are intended for use in the United States, where the manufacturer is based.
Catalogue
Uroflowmeter Ref K142425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Be Technologies, Inc. have in the registry?
The registry currently lists 1 device for Be Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Be Technologies, Inc.'s devices?
Among its 1 most recently registered device, Be Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Be Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Be Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Be Technologies, Inc. in the registry?
The most recently registered devices listed for Be Technologies, Inc. include Uroflowmeter.