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Sign in to claim this brandBe Technologies, Inc.
US
Last updated May 23, 2026
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.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Be Technologies, Inc. manufacture?
Be Technologies, Inc. specializes in uroflowmeters, which are diagnostic devices designed to measure urine flow rate and volume during voiding. These devices help clinicians evaluate urinary function and identify potential issues in the lower urinary tract.
Where is Be Technologies, Inc. based, and where are its devices intended for use?
Be Technologies, Inc. is headquartered in the United States, and its uroflowmeters are intended for use within that market. The company’s focus aligns with regulatory requirements and compliance frameworks applicable to the US healthcare system.
How are Be Technologies, Inc.’s uroflowmeters classified under FDA regulations?
Be Technologies, Inc.’s uroflowmeters are classified as Class II devices by the FDA. This classification is based on their role in diagnosing urinary function, which requires a higher level of scrutiny than Class I devices but does not pose the same risks as Class III devices. Class II devices typically require premarket notification (510(k)) clearance to demonstrate substantial equivalence to a legally marketed predicate device.
Which regulatory registries or databases list Be Technologies, Inc.’s uroflowmeters?
Be Technologies, Inc.’s uroflowmeters are listed via the FDA’s 510(k) clearance pathway, meaning they are included in the agency’s database of cleared devices. This pathway ensures that each device has been reviewed to confirm it meets FDA requirements for safety and effectiveness before being marketed in the US.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (50)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bio2 Technologies | 1000058 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000066 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000060 | FDA UDI | Class II | Active |
| Bio2 Technologies | 100-0259 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000038 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000037 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000045 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000046 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000055 | FDA UDI | Class II | Active |
| Bio2 Technologies | 100-0258 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000039 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000056 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000044 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000048 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000061 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000047 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000049 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000035 | FDA UDI | Class II | Active |
| Bio2 Technologies | 100-0130 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000070 | FDA UDI | Class II | Active |
| Bio2 Technologies | 100-0129 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000042 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000036 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000054 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000071 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000067 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000064 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000072 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000062 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000041 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000051 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000040 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000052 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000063 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000043 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000053 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000069 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000065 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000050 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000231 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000059 | FDA UDI | Class II | Active |
| Bio2 Technologies | 100-0132 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000232 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000057 | FDA UDI | Class II | Active |
| Bio2 Technologies | 1000068 | FDA UDI | Class II | Active |
| Bio2 CLM BG Bioactive Scaffold | K142463 | FDA 510(k) | Class II | Active |
| Bio2 CLM BG Bioactive Scaffold | K152589 | FDA 510(k) | Class II | Active |
| Bio2 Fusion Implant System | K151876 | FDA 510(k) | Class II | Active |
| S.E.A.L. Hemostatic Wound Spray | K210751 | FDA 510(k) | U | Active |
| Uroflowmeter | K142425 | FDA 510(k) | Class II | Active |
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