Profile: Mimosa Acoustics, Inc. manufactures state-of-the-art auditory diagnostic systems for evaluating middle and inner ear health. Our product HearID™ Auditory Diagnostic System provides user interface & patient database that evaluates the inner ear status without giving pressure to the ear. Our middle-ear power analyzer provides a non-invasive method for characterizing middle-ear transduction with acoustic power assessment. Our HearID auditory diagnostic system incorporates portable, lightweight hardware with a flexible, intuitive software interface. The measurement probe plugs directly into a laptop computer through a proprietary PC-card. The integrated user interface gives instant access to patient records and the customizable measurement modules. It measures middle-ear power reflectance, impedance, and related measures & measure transient-evoked otoacoustic emissions (TEOAEs) and distortion-product otoacoustic emissions (DPOAEs).
The company was founded in 1994 and is CE, FDA 510(k) certified.
FDA Registration Number: 2249246
11 Products/Services (Click for related suppliers)
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• Clinical Reflectance System |
• Distortion Product Otoacoustic Emission System |
• ENT Computer Software |
• Evoked Response Auditory Stimulator (FDA Code: GWJ / 882.1900) An evoked response auditory stimulator is a device that produces a sound stimulus for use in evoked response measurements or electroencephalogram activation. |
• HearIDT Auditory Diagnostic System |
• Infant Screening & Testing Units |
• Otoacoustic Emission Systems |
• Otoacoustic Emission Test Equipment |
• Stimulus-Frequency Otoacoustic Emission System |
• Transient-Evoked Otoacoustic Emission System |
• Wideband Acoustic Immittance System |